Mars Petcare US Announces Voluntary Recall of Limited Number of CESAR® Classics Filet Mignon Flavor Wet Dog Food

caeser524703Franklin, Tennessee — Today, Mars Petcare US announced a voluntary recall of a limited number of CESAR® Classics Filet Mignon Flavor product due to a potential choking risk from hard white pieces of plastic which entered the food during the production process. CESAR® Classics Filet Mignon can be purchased individually, as well as, in flavor variety multipacks. The Lot Codes listed below are the only affected products. All other CESAR® products can be safely consumed.

We encourage consumers who have purchased affected product to discard the food or return it to the retailer for a full refund or exchange. While a small number of consumers have reported finding the plastic pieces, to date, we have not received any reports of injury or illness associated with the affected product. The lot codes indicated below should not be sold or consumed.

Affected product was distributed to retail customers throughout the United States. Mars Petcare US is working with all of our distributors and retailers to ensure that the recalled products are no longer sold and are removed from inventory.

Recalled Pet Food

Two lot codes of CESAR® Classics Filet Mignon Flavor wet dog food with the production codes shown below are included in this voluntary recall. Each product will have a lot code printed on side of the tray that begins with 631FKKC, 631GKKC. A Best Before date 080418 (August 4, 2018) and 080518 (August 5, 2018).

The CESAR® Classics Filet Mignon Flavor can be found in variety packs with the following lot codes:

632D14JC, 633B24JC, 634A14JC, 634A24JC, 634B14JC, 634B24JC, 634E14JC, 635A24JC, 635B14JC, 636D24JC, 636E14JC

At Mars Petcare US, we take our responsibility to pets and their owners seriously. Pet owners who have questions about the recall should call 800-421-6456 between the hours of Saturday, October 8, 8:00 am to 12:00 pm CST and Monday through Friday 8:00 am to 4:30 pm CST or visit https://www.cesar.com/notice.

Vascular Solutions, Inc. Issues Recall of Twin-Pass® Dual Access Catheters

On September 16, 2016, Vascular Solutions, Inc., initiated a nationwide recall of Twin-Pass Dual Access catheters used in catheterization procedures. All unexpired lots of the product have been recalled because there is a potential for excess manufacturing material to remain at the tip of the catheter or within the distal portion of the rapid exchange lumen. It is possible that the excess material may separate from the catheter during use and pose a potential risk of embolism, which could result in serious injury or death. No injuries have been reported in association with this issue to date.

Healthcare facilities that have the affected Twin-Pass dual access catheters should remove the products from their inventory and return them to Vascular Solutions.

The recalled products were manufactured from October 2014 to August 2016 and distributed from October 2014 to September 2016.

The recalled products are all unexpired lots of Model Numbers 5200, 5210, and 5230. A listing of the recalled lots is available from Vascular Solutions and has been provided to each facility that purchased the affected products. A total of 15,896 devices have been manufactured, with 5,784 distributed in the United States and currently unexpired. The condition that led to the recall may affect approximately 9.2% of recalled devices.

Vascular Solutions, Inc. voluntarily initiated the recall on September 16, 2016 through an Urgent Medical Device Recall notification distributed to purchasers of the affected products. The notification identified the specific unexpired lots subject to the recall and included instructions on how to return the affected products.

The U.S. Food and Drug Administration (FDA) classified this as a Class I recall. FDA defines Class I recalls as “a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”

Consumers with questions may contact the company by phone at 1-888-240-6001 Monday through Friday, between the hours of 8:00 a.m. and 5:00 p.m. Central Time or by email at customerservice@vasc.com. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program Online at http://www.fda.gov/medwatch/report.htm (form available to fax (1-800-FDA-0178) or mail), or you may call the FDA at 1-800-FDA-1088 to request a reporting form.

Kraft Heinz Recalls Ready-To-Eat Lunchables Ham and American Cracker Stackers

lunch-1WASHINGTON D.C. — Kraft Heinz Company, a Fullerton, Calif. establishment, is recalling approximately 959 pounds of ready-to-eat “Lunchables Ham and American Cracker Stackers” packaged lunch products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains wheat and soy, known allergens, which are not declared on the product label.

The ready-to-eat meat and cheese packaged lunch items were produced on September 21, 2016. The following products are subject to recall:

3.4-oz. boxes containing four-compartment plastic trays of “Lunchables Ham and American Cracker Stackers,” with a “USE BY” date of 25 DEC 2016 and production times ranging from 9:13 to 10:00 stamped on the side of the plastic container.

The products subject to recall bear establishment number “EST. 537K” inside the USDA mark of inspection. These items were shipped to retail locations in Utah and California.
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The problem was discovered on October 6, 2016, when the firm received a consumer complaint. There were no illnesses associated with the complaint.

The establishment determined that the “Lunchables Ham and American Cracker Stackers” products were incorrectly labeled with the back label for a “Nacho Lunchable” product. The back label contains the product ingredient statements and as such, the “Lunchables Ham and American Cracker Stackers” products that were mislabeled do not declare wheat and soy on the label.

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

Consumers who have purchased this product are urged not to consume it. This product 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 the Kraft Heinz Consumer Relations Center, at 1-800-573-3877. Members of the media with questions about the recall can contact Lynne Gaila, Corporate Affairs Director, Kraft Heinz Company, at (847) 646-4396 or lynne.galia@kraftheinzcompany.com.

McCain Foods USA, Inc. Announces a Product Recall Impacting Frozen Onion Rings

Lisle, IL — McCain Foods USA, Inc. today announced it is voluntarily recalling retail, frozen onion ring products due to the use of incorrect packaging that does not declare milk as one of the ingredients. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products.

These frozen onion ring products are sold under the following brands/retail locations: Save-A-Lot Stores (40oz Bag of Frozen Breaded Diced Onion Rings, Premium Pick 5 Mix and Match Brand), Krasdale Brand (16oz Bag of Frozen Onion Rings), Spartan Brand (20oz Bag of Frozen Onion Rings) and Shur Fine Brand (16oz Bag of Frozen Onion Rings). No other products are impacted by this recall.

The products being recalled have been manufactured after October 20th, 2015 and prior to September 23, 2016. The production date code will begin with the letter “V” on the bag. Production date is documented on the bag via the following format: VYYMMDD. V=Production Plant Impacted By Recall. YY = Year. MM = Month. DD=Day.& Therefore, packages with date codes after October 20, 2015 [V151020] and prior to September 23, 2016 [V160923] are a part of the recall.
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Consumers who have an allergy or severe sensitivity to milk are advised to check their freezers and should throw out unused product or return any of it to the place of purchase for a full refund.

There have been no reported illnesses associated with the consumption of this product.

Food safety remains a top priority for McCain Foods USA, Inc. and we have full confidence that all appropriate steps are being taken to protect our consumers. McCain is working cooperatively with the FDA and retailers to ensure the affected products are removed from the marketplace.

Consumers with concerns or questions about the recall should contact McCain Foods at (630) 857-4329.

Get Set for the SET

During the Cascadia Rising earthquake exercise in the Pacific Northwest, Island County Amateur Radio Club members John Acton, K7ACT (seated, in yellow vest), types a Red Cross emergency message via a 2 meter packet link, while Bill Frederick, KF7BMK (standing, with handheld), monitors a VHF simplex voice net at a field triage and treatment facility on Whidbey Island. Red Cross volunteers Kendra O'Bryan (left) and Patty Cheek (right) help coordinate the message traffic flow. [Vince Bond, K7NA, photo]

During the Cascadia Rising earthquake exercise in the Pacific Northwest, Island County Amateur Radio Club members John Acton, K7ACT (seated, in yellow vest), types a Red Cross emergency message via a 2 meter packet link, while Bill Frederick, KF7BMK (standing, with handheld), monitors a VHF simplex voice net at a field triage and treatment facility on Whidbey Island. Red Cross volunteers Kendra O’Bryan (left) and Patty Cheek (right) help coordinate the message traffic flow. [Vince Bond, K7NA, photo]

The primary focal point of the 2016 ARRL Simulated Emergency Test (SET) is just ahead — Saturday and Sunday, October 1 and 2. The national emergency exercise is aimed at testing the skills and preparedness of the Amateur Radio Emergency Service (ARES) and other organizations that are called into action in actual emergency situations.

“Every local ARES team and/or ARRL Section will come up with their own scenarios and work with served agencies and partner organizations during the SET,” ARRL Field Organization Team Supervisor Steve Ewald, WV1X, said, noting that not all SETs will take place on October 1 and 2.

“SETs can be scheduled at the local and Section levels and conducted throughout the fall to help maximize participation,” he said. “But ARRL Field Organization leaders have the option of conducting their SETs on another weekend, if October 1 and 2 is not convenient.”

ARRL Field Organization leaders are among those tasked with developing plans and scenarios for this year’s SET, Ewald explained.

“The SET invites all radio amateurs to become aware of emergency preparedness and available training,” Ewald said. “ARES, Radio Amateur Civil Emergency Service (RACES), National Traffic System™, SKYWARN, Community Emergency Response Team (CERT), Salvation Army Team Emergency Radio Network (SATERN), and other allied groups and public service-oriented radio amateurs are encouraged to participate.”

The object of the annual nationwide exercise is to test training and skills and to try out new methods.

“It’s a time to work with partner organizations and served agencies to get to know them better and to determine their needs before an emergency or disaster strikes,” Ewald said. “Knowing who to contact within partner groups and knowing the planned procedures will help everyone to accomplish their goals and succeed in their missions.

Tyson Foods Inc. Recalls Chicken Nugget Products

WASHINGTON — Tyson Foods Inc., a Sedalia, Mo. establishment, is recalling approximately 132,520 pounds of fully cooked chicken nugget products that may be contaminated with hard plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

This is a Class I Recall which represents a health hazard where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.

The fully cooked Panko Chicken Nuggets items were produced on July 18, 2016. The following products are subject to recall:
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  • 5-lb. bag containing “Tyson FULLY COOKED PANKO CHICKEN NUGGETS” with a “Best If Used By” date of July 18, 2017 and case code 2006SDL03 and 2006SDL33.
  • 20-lb. bulk packages containing “SPARE TIME Fully Cooked, Panko Chicken Nuggets, Nugget Shaped Chicken Breast Pattie Fritters With Rib Meat” with a production date of July 18, 2016 and case code 2006SDL03.

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The products subject to recall bear establishment number “EST. 13556” printed adjacent to the “Best If Used By” date on the back of the package. The 20-pound cases were shipped for institutional use in Pennsylvania and the five-pound bags were shipped to retail locations nationally.

The problem was discovered after the firm received consumer complaints regarding foreign material contamination of chicken nugget products. According to Tyson Foods, the plastic material ranged in size from 21mm in length and 6.5mm in diameter and may have come from a round, hard plastic rod used to connect a plastic transfer belt. The firm said the products pass through a metal detector, but the plastic is not detectable to this technology.

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.

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.

Honeywell recalls one lot of Eyesaline Eyewash Solution

In cooperation with the U.S. Food and Drug Administration (FDA), Honeywell is voluntarily recalling one production lot of 32-ounce bottles of Eyesaline Eyewash solution, which is used for emergency eye rinsing after an injury.

Although no injuries have been reported and we have not found any contamination in our batch testing, the voluntary recall is a precautionary measure due to a low risk of product contamination with Klebsiella pneumoniae. Although found in the normal flora of the mouth and skin, if the contaminant were present in a bottle, there is a potential for it to result in infections that may be sight-threatening.

Eyesaline Eyewash is sold through industrial sales distributors. Approximately 9,700 32-ounce bottles with lot number F16091-61 are subject to recall. No other lot number of the product is subject to this recall.

All of Honeywell’s distributors who received this lot have been notified by phone, e-mail and certified mail, and have been instructed to notify their customers. See instructions below on how to find the lot number to determine if your supply is covered by this voluntary recall.

Distributors must stop distribution of the affected product and return it to Honeywell for credit or replacement.  Commercial-industrial users of the product should also check whether their Eyesaline Eyewash is subject to recall. If it is, customers should stop using the solution and contact their distributor for replacement or credit.
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The affected product and lot number can be identified as follows:

  • Product: 32 ounce Eyesaline Eyewash
  • Lot number:  F16091-61 (no other lot number is subject to recall)
  • The lot number can be found on the outside of the product case, shown at left, and on individual bottles, as shown on the right below.

Customers with questions regarding this recall can contact their distributor or Honeywell Customer Care at 1-800-430-5490, Monday – Friday, and 8:00 am – 6:30 pm EST.  Customers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this 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.

Perseid meteor shower going through tonight

The annual Perseid meteor shower will peak this Thursday night – Friday morning, August 11-12. This may be an above average year for the number of meteors.

The best time to watch for Perseid meteors will be from about 1 am (after the moon sets) until about 4 am at the first traces of daylight.

Perseus will be high in the northeast, but meteors should be visible over much of the sky. A dark observing site will be best.

ConAgra Foods Recalls Frozen Chicken and Beef Products Due to Possible Foreign Matter Contamination

ConAgra-3 ConAgra Foods, a Russellville, Ark. establishment, is recalling approximately 3,806 pounds of frozen chicken and beef entrée products that may be contaminated with extraneous materials, specifically metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The metal fragments range in size between 2 and 9 millimeters (mm) in diameter, and are curled, malleable and shiny. The metal fragments may be embedded in the sauce contained within the frozen entrée products.

The frozen chicken and beef entrée items were produced on June 13, 2016 and June 22, 2016. The following products are subject to recall: [View Labels (PDF only)]

* 22-oz. plastic bagged meal packages of “P.F. Chang’s Home Menu Brand Signature Spicy Chicken.” with “Use By” date of 6/08/17 and case code 5006616500.
* 22-oz. plastic bagged meal packages of “P.F. Chang’s Home Menu Brand Mongolian Style Beef.” with “Use By” date of 6/17/17 and case code 5006617400.

The products subject to recall bear establishment number “EST. 233” or “EST. P-115” inside the USDA mark of inspection. These items were shipped to distributors and retail locations in Arkansas, Illinois, Michigan, Minnesota, New York, Vermont, and Wisconsin.

The problem was discovered July 1, 2016, when an establishment employee observed metal fragments while dispensing sugar from a supplier for sauce formulation during processing. The resulting sauce is a component in the frozen entrée products.

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

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.

The 13 Colonies Special Event Gets Under Way tomorrow

militia-01The Amateur Radio Relay League announces a special Independence week event. The event consists of contacting stations in all of the original thirteen colonies. This is a great way to spend Independence Day and a great way to introduce your friends to amateur radio.

The eighth annual 13 Colonies Special Event takes place from 1300 UTC on July 1 until 0400 UTC on July 7. Stations working the special event station in at least one of the original 13 states — or all 15 participating stations — will be eligible for a certificate. A Liberty Bell endorsement will be attached for stations contacting sister special event station WM3PEN, in Philadelphia, where independence was declared. Back this year, is a second sister station GB13COL in Durham, England.

Stations will be on the air from each of the original 13 colonies — Connecticut (K2D), Delaware (K2E), Georgia (K2G), Massachusetts (K2H), Maryland (K2F), North Carolina (K2J), New Hampshire (K2K), New Jersey (K2I), New York (K2A), Pennsylvania (K2M), Rhode Island (K2C), South Carolina (K2L), and Virginia (K2B). All HF bands and all modes will be in play, with the exception of 60 meters. Operation on 2 and 6 meter simplex is encouraged.