Category Archives: National

What is this Amateur Radio?

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Glen Davis, KG7YDJ

An amateur radio operator, Yvette Cendes, KB3HTS. Wikipedia photo

You might have heard of Amateur—or “Ham”—radio, but do not really know what it is about. You may be familiar with Citizens Band, or CB, radio and have seen it in movies. Perhaps you purchased those bubble packs of walkie-talkies off of the shelves at Walmart. These are nothing compared to amateur radio. This article will attempt to explain the differences between these radio services and how you can obtain a license.

We should explain where you can find the rules about the radio services, first. The radio services and radios mentioned above are regulated by the Federal Communications Commission. The regulations are found in the Code of Federal Regulations. You can simply search for 47 C.F.R. and you will find all of the FCC regulations. Part 97 of those regulations cover Amateur Radio and Part 95 of those regulations cover CB and other radio services. “In the business,” we simply refer to Part 95 or Part 97.

We will start with a brief explanation of Part 95. The regulations for Citizens Band, General Mobile Radio Service (GMRS) and Family Radio Service (FRS) are covered in Part 95. There is another little used radio called Multi-Service Radio Service (MURS). CB, FRS and MURS are “licensed by rule.” That means that you can use these services without getting a “hard copy” license from the FCC. If you break the rules in Part 95, however, the FCC can track you down and fine you and order you to stop using them.

You are required to get a license from the FCC to use the GMRS frequencies. Even if you have those walkie-talkies you purchased from Walmart a few years ago. On some of those radio they combined FRS and GMRS channels. To use the GMRS channels, you are required to get a license. The reason is that GMRS uses more power than the other services and can use some features found in amateur radio. A ten-year license costs $75. Only the head of the household needs to obtain the license and all family members can use the same call sign assigned by the FCC.

The difference between the aforementioned radio services and amateur radio is power. Amateur radio uses more power and a broader spectrum of frequencies. You are not allowed to modify Part 95 radios discussed above. In amateur radio, however, you can modify radios for special uses and even build your own radio.

Amateur radios can be used to control radio controlled planes, robots, cars, boats or whatever. Although you cannot use the full power of amateur radio for this purpose, you can use more power than the controllers that come with normal models you put together giving you longer range.

Amateur radio can be used with the Internet to allow you to connect to different locations around the world. With the appropriate license, you can use amateur radio frequencies and power to contact people direct. You can also use radio frequencies and equipment to send and receive digital messages and send emails. You can use a simple handy talkie (HT)—what amateurs call walkie-talkies—to talk through satellites.

Amateur radio operators set up a trailer in Flagstaff to continue emergency communications as the Museum Fire threatened communication facilities on Mt. Elden.

There is more to amateur radio, but on a more practical level all of these radio services can be used in an emergency. In fact, anyone can use any radio service to call for help to prevent “…the immediate loss of life or property.” Amateur radio is used at the Emergency Operation Center in Flagstaff. At the beginning of the Tinder Fire in 2018, cell phones were useless. An amateur radio operator sent evacuation notices from the scene to the Emergency Operation Center in Flagstaff.

There are three-levels of amateur radio licenses. From lowest to highest they are Technician, General and Amateur Extra. You are NOT required to learn Morse code for any of the licenses. Most people are happy with a Technician license because you can do a lot even though you are limited in frequency privileges. The General license gives you access to most of the frequencies available in the amateur radio portion of the spectrum. The Amateur Extra is much harder to obtain and gives you just a few more frequency privileges over the General.

We should point out that you are not allowed to use any of the radio services if you have a felony conviction on your record. If you get your rights restored, however (which is not difficult to do), you can obtain a license. It might take a little longer.

Another thing about amateur radio is you are NOT required to join any club or participate in emergency communication programs, such as the Amateur Radio Emergency Service, to use the radio. Once you are licensed, you can use the frequencies appropriate to your license level. It is intended, first and foremost, as a fun hobby.

For more information you can consult the following web sites:
Amateur Radio Relay League
Bill Williams Mountain Radio Club
Coconino Amateur Radio Club

FEMA and FCC Conduct Nationwide Emergency Alert System Test

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WASHINGTON – FEMA, in coordination with the Federal Communications Commission, will conduct a nationwide test of the Emergency Alert System (EAS) on Wednesday, August 7, 2019.

The nationwide test will be sent to radio and television stations beginning at 2:20 p.m. EDT.

The test is being conducted through FEMA’s Integrated Public Alert and Warning System (IPAWS). This year, the test message will originate from designated radio stations, known as Primary Entry Point stations, which participate in a component of IPAWS called the National Public Warning System.

All other radio and television stations, cable, wireline service providers, and direct broadcast satellite service providers should subsequently receive and broadcast the test message.

This year’s test will evaluate the readiness of the national alerting capability in the absence of internet connectivity. The test will be approximately one minute long, have a limited impact on the public with only minor interruption of radio and television programs, and will be similar to regular monthly EAS tests. Both the audio message and text crawl should be accessible to people with disabilities.

The test will not include a message on cell phones via Wireless Emergency Alerts.

Enter for your chance to win $5,000 and publication in a short story anthology.

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Borders. Boundaries. Limits. Life is a continual process of crossing borders and discovering something new. Tell us stories about overcoming obstacles; of physical, spiritual, and emotional change and growth.

Lulu is an Internet self-publishing book company. Authors can upload books, manage the covers and order copies for distribution. Set-up is free and the books are made available for purchase online. Lulu is currently seeking short stories for a chance to be published in an their upcoming anthology on change.

Lulu’s $5k for 5k contest seeks original works of fiction and non-fiction that center on the theme “Crossing Borders.” Entries should clearly tie to the ideas of change and transition with an emphasis on crossing borders.

Submission Requirements

  • Submissions must be received during the contest period from 4/1/19 at 12:01 am ET to 6/30/19 at 11:59 pm ET.
  • Entries should clearly tie to the ideas of change, and transition with an emphasis on crossing borders. Both fiction and non-fiction entries will be accepted.
  • All entries must be between 2,000 and 5,000 words.
  • All entries must contain only original content. The author must own all rights to the content. Content includes both images and text. No copyright text or images. Quotes and licensed images must be properly attributed.
  • All entries must be submitted through the form below as a PDF or DOCX attachment. Limit one submission per author please.
  • Entrants must be 18 years or older. U.S. residents only.

Enter for your chance to win $5,000 and publication in a short story anthology.
Prizes

  • Grand Prize Winner will receive $5,000, plus a ticket to BookCon 2020 in NYC.
  • Shortlisted submissions will be included in the Crossing Borders Anthology, get a free copy of the anthology, and get Lulu swag.

Medex Cardio-Pulmonary Recalls Sterile Saline and Sterile Water

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The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death

Recalled Product(s):

  • Select serial and lot numbers of Smiths Medical Sterile Saline and Water (listed below)
  • Manufacturing Dates: August 30, 2013, to February 10, 2017
  • Distribution Dates: August 30, 2013, to February 10, 2017
  • Full list of affected devices
  • Devices Recalled in the U.S.: 939,364

Device Use

The sterile saline and water are respiratory humidification products used in patients undergoing respiratory therapy, tracheal wash, or wound cleaning.

Reason for Recall

Smiths Medical is recalling the sterile saline and sterile water products for inhalation due to the potential exposure to infectious agents (bacillus infantis and staphylococcus epidermidis) because of damage to the containers used to package the finished products. Use of these products in patients could result in infection and may require treatment with antibiotics. Serious or untreated infections could result in patient death.

The company initiated a voluntary recall on September 5, 2017. That recall covered several products, including some that are outside the scope of this notice. The FDA is auditing the recall to ensure the company has notified all affected customers and that affected product has been returned. Based on the available information, the FDA is now classifying the action regarding the affected products (listed below) as a Class I recall.

Who May be Affected

  • Hospitals and health care professionals using Smiths Medical Sterile Saline or Water distributed from August 30, 2013, to February 10, 2017.
  • Patients receiving respiratory therapy or tracheal lavage with Smiths Medical Sterile Saline or Water distributed from August 30, 2013, to February 10, 2017.

What to Do

On September 5, 2017, Smiths Medical sent affected customers an “Urgent Medical Device Recall Notice” informing them of affected sterile water and saline product models and directing them to locate, determine the affected sterile saline or water products in their possession, and to complete the “Urgent Medical Device Recall Response Form” attached to the recall notice. Customers were also instructed to return all affected product to Stericycle for processing.

On January 7, 2019, distributer Medline Industries Inc. initiated a sub-recall for privately labeled product models and lots, affected by the September 5, 2017, Smiths Medical recall notice, that were not expired and which may be potentially contaminated with the infectious agents.

The notice asked customers to:

  1. Locate the affected Sterile Water, Saline and Eye Wash in their possession by referring to the specific model and lot numbers listed in the Urgent Medical Device Field Recall Response Form.
  2. Determine the number of affected devices in their possession and complete the Urgent Medical Device Field Recall Response Form attached to this letter within 10 days of receipt and send it to smithsmedicalste00100@stericycle.com. The form must be returned even if customers do not have any of the affected Sterile Water, Saline and Eye Wash in their possession. Product credit will be processed once the Urgent Medical Device Field Recall Response Form and affected product is received. All affected devices must be returned to Stericycle for processing. Pre‐paid shipping labels were included with the Urgent Medical Device Recall Notice.
  3. Package the affected devices and include a copy of the completed Urgent Medical Device Field Recall Response Form inside EACH BOX of the returned devices to obtain credit for the returned devices. Make sure boxes are sealed and labeled with the facility name prior to shipping devices to Stericycle.

Distributors are asked to immediately notify customers who received the affected product of this Recall.

Contact Information

Customers with questions regarding this notification may contact Stericycle via email at smithsmedicalste00100@stericycle.com.

Date Recall Initiated

September 5, 2017

Full List of Affected Devices

  • Portex 350 ml Sterile Water Humidifier w/5psi Adapt (Model # 352 Lot Numbers: A214, A215, Z263, Z532, and Z555)
  • Portex 550 ml Sterile Water Humidifier w/5psi Adapt (Model # 552 Lot Numbers: A054, A089, A090, and Z262)
  • Portex 1000 ml Sterile Water USP Pour Bottle (Model # 1065 Lot Numbers: B209 and Z225)
  • Portex 500 ml Sterile Water USP Pour Bottle (Model # 1565 Lot Number: Y371)
  • Intermed 350 ml Sterile Water Humidifier w/5psi Adapt. (Model # 0352IMJ Lot Numbers: A457, A597, B157, B236, Z589, Z655, Z656, and Z661)
  • Portex 550 ml Sterile Water Humidifier w/5psi Adapt. (Model # 0552C Lot Number: Z370)
  • Intermed 550 ml Sterile Water Humidifier w/5psi Adapt. (Model # 0552IMJ Lot Numbers: Z588 and Z597)
  • Medline 300-350 ml Sterile Water Humidifier w/5psi Adapt. (Model # HCS00300 Lot Number: Y576)
  • Medline Prefilled 350 ml Sterile Water (Model # HCS00350 Lot Numbers: A055, A056, A057, A058, A103, A176, A455, B530, B531, B532, B533, Z101, Z534, Z553, and Z554)
  • Portex Unit Dose 5 ml Normal Saline (0.9%) (Model # R0059 Lot Number: B360), K820227
  • Portex Unit Dose 15 ml Normal Saline (Model # R0159 Lot Numbers: A661, B067, A526, A536, A569, and B201)
  • Portex 5ml Normal Saline (0.9%) Unit Dose (Model # UD9005 Lot Number: B515), K820227
  • Medline Prefilled 550 ml Sterile Water (Model # HCS00550 Lot Numbers: A092, B205, B534, and Z205)

How do I report a problem?

Health care professionals and consumers may report adverse reactions or quality problems they experienced using these devices to MedWatch: The FDA Safety Information and Adverse Event Reporting Program. Health care professionals employed by facilities that are subject to FDA’s user facility reporting requirements should follow the reporting procedures established by their facilities.

Tris Pharma, Inc Expands Its Voluntary Nationwide Retail Recall of Ibuprofen Oral Suspension Drops

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Monmouth Junction, NJ, Tris Pharma, Inc. is expanding the scope of its November 2018 recall by adding three (3) additional lots of Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 mL, to the retail (pharmacy) level. Some units from these batches have been found to have higher levels of Ibuprofen concentration.

Infants already susceptible to the adverse effects of ibuprofen may be at a slightly higher risk if they receive medication from an impacted bottle. There is a remote probability that infants, who may be more susceptible to a higher potency level of drug, may be more vulnerable to permanent NSAID-associated renal injury. Some units from these six (6) lots have been found to contain Ibuprofen as high as 10% above the specified limit. Studies have shown that safety issues or toxicity is generally accepted to be a concern in infants at doses in excess of 700% of the recommended dose.1 To date, no serious adverse events have been reported related to this recall.

The product is used as a pain reliever/fever reducer and is packaged in ½ oz. and 1 oz. bottles. This voluntarily recall includes the six (6) lots listed below:

Lot No. NDC EXPIRATION DESCRIPTION COMPANY
4718 59779-925-23 12/19 CVS Health: Infants’ Ibuprofen Concentrated Oral Suspension, USP, 50 mg per 1.25 mL, in 0.5 oz. bottle CVS Pharmacy
00717005A 49035-125-24 02/19 Equate: Infants’ Ibuprofen Concentrated Oral Suspension, USP, 50 mg per 1.25 mL, in 1.0 oz. bottle Wal-Mart Stores Inc.
00717006A 59779-925-24 

(Labeled as: 50428-1252-4)

 02/19 CVS Health: Infants’ Ibuprofen Concentrated Oral Suspension, USP, 50 mg per 1.25 mL, in 1.0 oz. bottle CVS Pharmacy
00717009A
(Previously announced) 		49035-125-23 02/19 Equate: Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 ml, in 0.5 oz. bottle Wal-Mart Stores Inc
00717015A
(Previously announced) 		49035-125-23 04/19 Equate: Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 ml, in 0.5 oz. bottle Wal-Mart Stores Inc
00717024A
(Previously announced) 		49035-125-23 08/19 Equate: Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 ml, in 0.5 oz. bottle Wal-Mart Stores Inc
59779-925-23 CVS Health: Ibuprofen Oral Suspension Drops,
USP, 50 mg per 1.25 ml, in 0.5 oz. bottle		 CVS Pharmacy
55319-250-23 Family Wellness: Ibuprofen Oral Suspension Drops,
USP, 50 mg per 1.25 ml, in 0.5 oz. bottle		 Family Dollar Services Inc.

Tris Pharma, Inc. manufactures Ibuprofen Oral Suspension Drops, USP for a single customer, who markets and distributes the product to retailers. The retailers should stop further distribution of the affected lots, which are being recalled. Tris Pharma, Inc. has notified its customer by urgent recall notice and has arranged for the return of recalled products from retailers and distributors.

Consumers with questions regarding this recall may contact Tris Customer Service by 732-940-0358 (Monday through Friday, 8:00 AM ET- 5:00 PM PT) or via email at micc_tris@vigilarebp.com. Consumers, who may be concerned, should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA). The FDA has approved a class II retail level recall for this recall,

Tyson Foods, Inc. Recalls Chicken Nugget Products due to Possible Foreign Matter Contamination

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WASHINGTON DC – Tyson Foods, Inc., a Sedalia, Mo. establishment, is recalling approximately 36,420 pounds of chicken nugget products that may be contaminated with extraneous materials, specifically rubber, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The panko chicken nugget items were produced on Nov. 26, 2018. The following products are subject to recall:

5-lb. plastic packages of “Tyson WHITE MEAT PANKO CHICKEN NUGGETS” with a “BEST IF USED BY” date of “NOV 26 2019,” case code “3308SDL03” and time stamps 23:00 through 01:59 (inclusive).

The products subject to recall bear establishment number “P-13556” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.

The problem was discovered when the establishment received consumer complaints of extraneous material in purchased Panko Chicken Nugget products. FSIS was notified on Jan. 29, 2019.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

FSIS is concerned that some product may be frozen and in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers with questions about the recall can contact Tyson Consumer Relations at 1-888-747-7611. Members of the Media with questions about the recall can contact Worth Sparkman, Senior Communications Manager with Tyson Foods, Inc., at (479) 290-6358.

Hill’s Pet Nutrition Voluntarily Recalls Select Canned Dog Food for Excessive Vitamin D

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Hill’s Pet Nutrition is voluntarily recalling select canned dog food products due to potentially elevated levels of vitamin D. While vitamin D is an essential nutrient for dogs, ingestion of elevated levels can lead to potential health issues depending on the level of vitamin D and the length of exposure, and dogs may exhibit symptoms such as vomiting, loss of appetite, increased thirst, increased urination, excessive drooling, and weight loss. Vitamin D, when consumed at very high levels, can lead to serious health issues in dogs including renal dysfunction. Pet parents with dogs who have consumed any of the products listed and are exhibiting any of these signs should contact their veterinarian. In most cases, complete recovery is expected after discontinuation of feeding.

In the United States, the affected canned dog foods were distributed through retail pet stores and veterinary clinics nationwide. No dry foods, cat foods, or treats are affected.

Pet parents who purchased the product with the specific lot/date codes listed should discontinue feeding and dispose of those products immediately or return unopened product to your retailer for a refund. For more information, please contact Hill’s via our website or at 1-800-445-5777.

Hill’s Pet Nutrition learned of the potential for elevated vitamin D levels in some of our canned dog foods after receiving a complaint in the United States about a dog exhibiting signs of elevated vitamin D levels. Our investigation confirmed elevated levels of vitamin D due to a supplier error.

We care deeply about all pets and are committed to providing pet parents with safe and high quality products. Hill’s has identified and isolated the error and, to prevent this from happening again, we have required our supplier to implement additional quality testing prior to their release of ingredients. In addition to our existing safety processes, we are adding our own further testing of incoming ingredients.

For further information, please contact Hill’s Pet Nutrition, Inc. at 1-800-445-5777 Monday-Friday during the hours of 9am-5pm (CST) or at contactus@hillspet.com. Information can also be found at www.hillspet.com/productlist

This voluntary recall only impacts canned dog food and primarily in the United States. It is being conducted in cooperation with the U.S. Food and Drug Administration. Impacted products outside of the United States will be subject to separate notices on the country-specific website. If you are outside of the United States, please check your own country’s Hill’s website for more information.

Product Name SKU Number Lot Code/Date Code
Hill’s® Prescription Diet® c/d® Multicare Canine Chicken & Vegetable Stew 12.5oz 3384 102020T10
102020T25
Hill’s® Prescription Diet® i/d® Canine Chicken & Vegetable Stew 12.5oz 3389 102020T04
102020T10
102020T19
102020T20
Hill’s® Prescription Diet® i/d® Canine Chicken & Vegetable Stew 5.5oz 3390 102020T11
112020T23
122020T07
Hill’s® Prescription Diet® z/d® Canine 5.5oz 5403 102020T17
112020T22
Hill’s® Prescription Diet® g/d® Canine 13oz 7006 112020T19
112020T20
Hill’s® Prescription Diet® i/d® Canine 13oz 7008 092020T30
102020T07
102020T11
112020T22
112020T23
Hill’s® Prescription Diet® j/d® Canine 13oz 7009 112020T20
Hill’s® Prescription Diet® k/d® Canine 13oz 7010 102020T10
102020T11
Hill’s® Prescription Diet® w/d® Canine 13oz 7017 092020T30
102020T11
102020T12
Hill’s® Prescription Diet® z/d® Canine 13oz 7018 102020T04
112020T22
Hill’s® Prescription Diet® Metabolic + Mobility Canine Vegetable & Tuna Stew 12.5oz 10086 102020T05
102020T26
Hill’s® Prescription Diet® w/d® Canine Vegetable & Chicken Stew 12.5oz 10129 102020T04
102020T21
Hill’s® Prescription Diet® i/d® Low Fat Canine Rice, Vegetable & Chicken Stew 12.5oz 10423 102020T17
102020T19
112020T04
Hill’s® Prescription Diet® Derm Defense® Canine Chicken & Vegetable Stew 12.5oz 10509 102020T05
Hill’s® Science Diet® Adult 7+ Small & Toy Breed Chicken & Barley Entrée Dog Food 5.8oz 4969 102020T18
Hill’s® Science Diet® Puppy Chicken & Barley Entrée 13oz 7036 102020T12
Hill’s® Science Diet® Adult Chicken & Barley Entrée Dog Food 13oz 7037 102020T13
102020T14
112020T23
112020T24
Hill’s® Science Diet® Adult Turkey & Barley Dog Food 13oz 7038 102020T06
Hill’s® Science Diet® Adult Chicken & Beef Entrée Dog Food 13oz 7040 102020T13
Hill’s® Science Diet® Adult Light with Liver Dog Food 13oz 7048 112020T19
Hill’s® Science Diet® Adult 7+ Chicken & Barley Entrée Dog Food 13oz 7055 092020T31
102020T13
Hill’s® Science Diet® Adult 7+ Beef & Barley Entrée Dog Food 13oz 7056 092020T31
112020T20
112020T24
Hill’s® Science Diet® Adult 7+ Turkey & Barley Entrée 13oz 7057 112020T19
Hill’s® Science Diet® Adult 7+ Healthy Cuisine Braised Beef, Carrots & Peas Stew dog food 12.5oz 10452 102020T14
102020T21
Hill’s® Science Diet® Adult 7+ Youthful Vitality Chicken & Vegetable Stew dog food 12.5oz 10763 102020T04
102020T05
112020T11

Jennie-O Turkey Store Sales, LLC Recalls Raw Ground Turkey Products

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WASHINGTON D.C. — Jennie-O Turkey Store Sales, LLC, a Barron, Wis. establishment, is recalling approximately 91,388 pounds of raw ground turkey products that may be associated with an illness outbreak of Salmonella Reading, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The raw ground turkey products items were produced on September 11, 2018. The following products are subject to recall:

  • 1-lb. packages of “Jennie-O GROUND TURKEY 93% LEAN | 7% FAT” with “Use by” dates of 10/01/2018 and 10/02/2018.
  • 1-lb. packages of “Jennie-O TACO SEASONED GROUND TURKEY” with a “Use by” date of 10/02/2018.
  • 1-lb. packages of “Jennie-O GROUND TURKEY 85% LEAN | 15% FAT” with a “Use by” date of 10/02/2018.
  • 1-lb. packages of “Jennie-O ITALIAN SEASONED GROUND TURKEY” with a “Use by” date of 10/02/2018.

The products subject to recall bear establishment number “P-190” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.

FSIS, and its public health partners, including the Centers for Disease Control and Prevention (CDC) and the Arizona Department of Health Services, have been conducting traceback activities for a sample of Jennie-O brand ground turkey in an intact, unopened package from a case-patient’s home. The patient tested positive for Salmonella Reading and the sample from the ground turkey matches the outbreak strain.

FSIS, the CDC, and state public health and agriculture partners, have been working together on an illness cluster involving 164 case-patients in 35 states. Patients have reported eating different types and brands of turkey products purchased from many different stores, handling raw turkey pet food and/or raw turkey, or working with live turkeys or living with someone who handled live turkeys. FSIS continues to work with the CDC and state health departments on this investigation and will provide updated information as it becomes available. Based on the continuing investigation, additional product from other companies may also be recalled.

Consumption of food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 12 to 72 hours after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop a severe illness. Individuals concerned about an illness should contact their health care provider.

FSIS is concerned that some product may be frozen and in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.

FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume raw poultry product that has been cooked to a temperature of 165°F. Safe steps in food handling, cooking, and storage are essential in preventing foodborne illness. You can’t see, smell, or taste harmful bacteria that may cause illness. In every step of food preparation, follow the four guidelines to keep food safe:

  • Clean—Wash hands and surfaces often.
  • Separate—Separate raw meat from other foods.
  • Cook—Cook to the right temperature.
  • Chill—Refrigerate food promptly.

Consumers with questions regarding the recall can contact Jennie-O Consumer Engagement Team at 1-800-621-3505, 8 a.m. to 4 p.m. Central Time Monday – Friday and 9 a.m. to 5 p.m. Central Time Saturday and Sunday. Media with questions can contact media@hormel.com or 507-434-6352.

Consumers with food safety questions can “Ask Karen,” the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at: https://www.fsis.usda.gov/reportproblem.

Stage II fire restrictions and Bill Williams Mountain closure remain in effect on Kaibab National Forest despite recent rain

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WILLIAMS — While the Kaibab National Forest received some rain over the weekend, forest managers would like to remind visitors that fire danger levels continue to be elevated and that Stage II fire restrictions as well as an area closure of the Bill Williams Mountain watershed will remain in place until much more significant and widespread precipitation is received.

Officials emphasize that the Kaibab National Forest is still at the height of its fire season and that northern Arizona continues to have the potential for large, severe wildfires. The Kaibab National Forest needs the public’s continued support in preventing unwanted, human-caused wildfires.

“We have had excellent compliance with the fire restrictions and area closure that are already in place on the Kaibab National Forest,” said Jerry Parker, Forest Service law enforcement officer. “Members of the public can continue to do their part in protecting our forests by remaining vigilant and abiding by all fire restrictions and area closures.”

The Forest Service uses fire restrictions and closures to help prevent unwanted, human-caused wildfires and to limit the exposure of visitors during periods of potentially dangerous fire conditions.

Forest officials remind visitors that having a campfire on the National Forest while under fire restrictions is a violation of law requiring a mandatory appearance in federal court and consequent fines and possible jail time. Visitors should use extra caution when recreating on all public lands during times of the year when fire danger is increased.

For detailed information about the Stage II fire restrictions and the area closure of the Bill Williams Mountain watershed currently in effect on the Kaibab National Forest, reference the following sources:

Website: www.fs.usda.gov/kaibab
Twitter: www.twitter.com/KaibabNF (Text ‘follow kaibabnf’ to 40404 to receive text messages.)
Facebook: www.facebook.com/KaibabNF
Arizona Fire Restrictions: firerestrictions.us/az

Wildfire start in Sycamore Canyon Wilderness

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SEDONA – Coconino National Forest firefighters are responding to a 40-acre wildfire approximately 9 miles northwest of Sedona growing in Sycamore Canyon Wilderness.

The human-caused Sycamore Fire was reported at about 10:20 a.m. today near Taylor Cabin Trail and is producing smoke that will be noticeable to those in the immediate area, burning primarily in pinyon juniper in the wilderness area.

Firefighting resources include four helicopters, five crews, and three engines—totaling approximately 100 personnel.

No structures are immediately threatened at this time and the wildfire is moving in the northeast direction. More information will be provided about this wildfire as it becomes available.