Category Archives: National Government

Maintenance work to begin on Forest Road 110 on Williams Ranger District

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WILLIAMS – A contractor working for the Kaibab National Forest will begin a road maintenance project May 21 on Forest Road 110 on the Williams Ranger District in order to ensure the popular route continues to meet Forest Service road standards.

This work will include basic maintenance, replacement of gravel, and cleaning out of culverts. The section of FR 110 to receive this maintenance work begins at the intersection of County Road 73, also known as Perkinsville Road, and continues until just before the intersection with FR 109.

Forest Service road engineers expect the road maintenance work to continue for about four weeks and likely be complete by June 19. While the road will not be closed during the project, motorists can expect delays and should exercise caution while traveling through the area due to varying road conditions and the presence of heavy equipment.

FR 110 is used frequently by Kaibab National Forest visitors to access camping, hunting and other recreational opportunities. Forest visitors seeking a spot for dispersed camping are encouraged to consider other routes on the Williams Ranger District during the duration of the road maintenance work given the likelihood of dust and noise near the project area.

Forest Service engineers regularly evaluate and monitor road conditions across the forest to determine priorities for work. FR 110 has been in need of maintenance for some time, and forest managers expect visitors to have an improved experience once the current project is complete.

To contact the Williams Ranger District office, call (928) 635-5600. Additional Kaibab National Forest is available through the following sources:

Facebook: www.facebook.com/KaibabNF/
Twitter: www.twitter.com/kaibabnf (Text ‘follow kaibabnf’ to 40404 to receive text messages.)
Kaibab website “News & Events”: www.fs.usda.gov/kaibab

Lamb Weston Issues Allergy Alert on Undeclared Milk in Red Robin Burgers and Brews Crispy Onion Rings Sold in Grocery Stores

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Lamb Weston is recalling 14 ounce packages of Red Robin Burgers and Brews Crispy Onion Rings manufactured by Fry Foods and sold in grocery stores, because the product may contain an undeclared milk allergen. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.

These products are NOT served in Red Robin restaurants. The Red Robin Burgers and Brews Crispy Onion Rings were distributed in the U.S. through retail grocery stores. No other products are impacted by this recall.

The product comes in a 14 ounce bag and is frozen. Details on the impacted packages are listed below. The Sell By Date and Package Code can be found on the back of the package. The HH:MM portion of the Package Code indicates the time product was made and will vary by package. Please refer to the images of the packaging included for additional information.

UPC Product Name Net Weight Sell By Dates Package Code
0 43301 61119 3 Red Robin Crispy Onion Rings 14 Oz Sell By OCT 28 2018
Sell By OCT 29 2018		 6906711841 HH:MM
6906711941 HH:MM

No illnesses have been reported to date in connection with this product.

The recall was initiated after it was discovered that contract manufacturer Fry Foods mistakenly packed product containing milk in packaging that did not reveal the presence of milk. Subsequent investigation indicates the product did not meet Lamb Weston specifications.

Consumers who have purchased Red Robin Burgers and Brews Crispy Onion Rings from a grocery retailer are urged to return the product to the place of purchase for a full refund.

Fry Foods and Lamb Weston are cooperating with the FDA on this recall and working with customers to ensure packages are removed from store shelves and are no longer distributed.

Consumers with questions about this recall may contact 1-866-518-0137, Monday-Friday, from 9 a.m. – 6p.m. EDT.

Trident Seafoods Corporation Recalls Frozen Multi-Grain Alaskan Cod

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Trident Seafoods Corporation is issuing a voluntary recall of select lots of frozen Multi-Grain Alaskan Cod, Net Wt. 12, oz., because they may contain small pieces of plastic. Consumption of these products may pose a choking hazard or other physical injury to the mouth.

The following retail product is subject to the voluntary recall:

Trident Seafoods Multi-Grain Alaskan Cod (Frozen), Net Wt. 12oz., UPC 0 28029 21048 4

Recalled Lot Numbers with associated Best By dates are printed on one end of the individual retail cartons and on the case label.

• Lot Number A633511, Best By: 11/30/2018
• Lot Number A636225, Best By: 12/27/2018

Lot Number A633511 – Distributed between 12/1/2016 and 2/9/2017 to Arizona, California, Colorado, Illinois, Kansas, Massachusetts, Minnesota, New Jersey, Pennsylvania, Texas, Washington, and Wisconsin

Lot Number A636225 – Distributed between 1/23/2017 and 2/17/2017 to Arizona, California, Colorado, Illinois, Kansas, Massachusetts, Texas, Washington, and Wisconsin

These products are sold at Albertsons, Amazon, Cub Foods, Jewel, Morey’s, Plaza Extra, Shaw’s, Shoprite, Sprouts, SUPERVALU, and Woodman’s retailers.

This issue was discovered through consumer feedback. The source of the white plastic has been identified as inspection tags used by an ingredient supplier. Trident Seafoods takes food safety very seriously and is investigating this situation thoroughly.

There have been no reports of injury or illness related to the recalled products to date, however 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. For additional information consumers can call Ms. Trev Foley, Consumer Affairs Manager, at 206-297-5825, Monday – Friday, 8 a.m. – 5 p.m. PST, or send email to trevf@tridentseafoods.com .

Northern Arizona federal land managers invite public to community conversation event

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FLAGSTAFF – Federal land managers with the Forest Service, National Park Service and Bureau of Land Management invite the public to attend a community conversation in May as part of an ongoing effort to connect with the public and hear first-hand what people value about their public lands.

In partnership with the Museum of Northern Arizona, this event will be held in Flagstaff in the Branigar Hall at the Museum of Northern Arizona from 6-8 p.m. on Thursday, May 25. Seating is limited to 60-70 people at this free community event, so please RSVP by calling (928) 774-5213 or visit www.musnaz.org.

The following federal land managers will be in attendance and look forward to interacting with the public:

– Coconino National Forest Supervisor Laura Jo West,
– Kaibab National Forest Supervisor Heather Provencio,
– Flagstaff Area National Monuments Superintendent Kayci Cook Collins,
– Grand Canyon National Park Superintendent Chris Lehnertz, and
– BLM Phoenix District Manager Leon Thomas.

Speakers will provide introductory remarks, move to “talking circles” to interact and have conversations with community members, and conclude by reporting out and providing closing remarks.

This is a chance for the public to meet face-to-face with the leaders of organizations that manage federal lands in northern Arizona. The public is invited to attend this special event and share their thoughts on what they value about public lands now and into the future.

North Kaibab Ranger District to open campgrounds on May 15

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FREDONIA – Recreational campgrounds on the North Kaibab Ranger District will open May 15 and remain open until Oct. 15.

Both the Jacob Lake campground and the DeMotte campground will be open and available for public recreation and overnight camping. The Jacob Lake campground is located 30 miles southeast of Fredonia, Ariz. on U.S. Route 89A at roughly 7,900 feet. The DeMotte campground is located about 25 miles south of the Kaibab Plateau Visitor Center on Arizona Highway 67 at roughly 8,700 feet.

A complete list of amenities may be found at Recreation.gov by searching for the specific campground. Campers are reminded to be mindful of any rules associated with the campground and always maintain fire safety when making a campfire. To stay current with any fire restrictions in Arizona go to firerestrictions.us/az.

Additionally, the Kaibab Camper Village, which is privately owned and managed but surrounded by Kaibab National Forest, is also scheduled to be open from May 14 through Oct. 15. Kaibab Camper Village offers full RV hookups and tent sites, and is located just 40 miles from the Grand Canyon National Park North Rim. For more information on Kaibab Camper Village, please visit kaibabcampervillage.com or call 928-643-7804.

To make reservations at the Jacob Lake campground or the DeMotte campground, please visit Recreation.gov or call 877-444-6777. For additional information on all of the Kaibab National Forest recreational sites please visit fs.usda.gov/recmain/kaibab/recreation.

U.S. Deer Antler EX. & IM., INC. Announces The Recall Of Herbal Tea Varieties In Pouches

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U.S. Deer Antler Ex. & Imp., of Los Angeles, CA is recalling a variety of Herbal Teas prepared on premises between 4/1/17 and 4/30/17 in cooperation with an inspection made by the California Department of Public Health. The aforementioned Herbal Teas, especially those with low-acidity held at room temperature, were not produced according to approved guideline, making them susceptible to contamination by Clostridium botulinum.

Below are the product descriptions and photographs:

Products Packaging Cases
Herbal Tea Variety Batches prepared on premise between 4/1/17 – 4/30/17 120 ml/ Pouch 40 Pouches / Case

The Herbal Teas were distributed to individual customers and acupuncturists in California, Florida, Illinois, Maryland, North Carolina, Texas, and Virginia.

Symptoms of Clostridium botulinum typically begin with blurred or double vision followed by trouble speaking, swallowing; and progression to muscle weakness starting in the upper body, moving downward.  Botulism can lead to life-threatening paralysis of breathing muscles requiring support with a breathing machine (ventilator) and intensive care. http://www.cdph.ca.gov/HealthInfo/discond/Pages/Botulism.aspx

People experiencing these symptoms who have recently consumed these Herbal Teas should seek immediate medical attention.

In its ongoing cooperation with the California Department of Public Health, U.S. Deer Antler Ex. & Imp., Inc. has immediately segregated its entire inventory of Herbal Tea varieties, and is notifying consumers and customers not to consume potentially-contaminated product. Furthermore, U.S. Deer Antler Ex. & Imp. Inc. is voluntarily recalling all varieties of general Herbal Teas prepared on-site in the period of 4/1/17 to 4/30/17 to ensure consumer safety.

Consumers in possession of these products are to stop consumption and return unconsumed product to their original place of purchase.

U.S. Deer Antler Ex. & Imp., Inc. will be sending recall notices to all of its direct customers.  Please contact Joong W. Park (323) 735-9665 for further information.

ReFlow Medical Issues Recall of Specific Lots of Wingman35 Crossing Catheters

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WASHINGTON, D.C. – On April 22, 2017, ReFlow Medical initiated a lot-specific voluntary recall of the Wingman35 Crossing Catheters.

The FDA is classifying this as a Class 1 recall, the most serious recall situation where the patient is exposed to a reasonable likelihood of death or a serious injury. The Wingman35 Crossing Catheters have been found to exhibit tip splitting or separation, which has resulted in two adverse events. ReFlow has received 2 complaints of catheter-tip splitting and/or separation. A total of 2327 Wingman catheters are in distribution.

Tip splitting has the potential to lead to loss of device function. Tip separation may require medical intervention to retrieve a separated segment or may occlude blood flow to end organs.

The Wingman Crossing Catheters in this recall were distributed between January 2015 and March 2016.

ReFlow Medical has notified its customers and distributors by recall notification letters. The letters requested that all customers and distributors quarantine and discontinue use of all potentially affected units and return the affected product to the company as soon as possible for credit.

FDA and other regulatory agencies around the world have been notified of this action.

Consumers with questions may contact ReFlow Medical Customer Relations at 1-949-481-0399, Monday through Friday, between 8:00 a.m. and 4:30 p.m. Pacific time or by email at info@reflowmedical.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 either online, by regular mail or by fax. Complete and submit the report Online: www.fda.gov/medwatch/report.htm Regular mail or fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, and then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

Pentagon Exhibit Showcases Wounded Warriors’ Therapeutic Art

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By Paige LaPlant

MSgt (Ret) Justin Jordan discusses the art process with U.S. Navy VADM Raquel Bono, Director, Defense Health Agency, at the opening of the Wounded Warrior Healing Arts Exhibit at the Pentagon in Arlington, Virginia, on April 12, 2017. (DoD photo by Roger L. Wollenberg)

WASHINGTON, April 12, 2017 — Healing arts therapy for wounded warriors can have a profound impact on those who have post-traumatic stress disorder and traumatic brain injury, and it also educates the medical community on treating such signatures of war, the director of the Defense Health Agency said today at the opening of the 2017 Wounded Warrior Healing Arts exhibit at the Pentagon.

Navy Vice Adm. (Dr.) Raquel C. Bono spoke at the kickoff of the Pentagon Patriotic Arts Program’s newest display, which will grace the walls of Apex 1 and 2 on the Pentagon’s second floor for a year.

The exhibit reflects the therapeutic artwork of service members who have suffered such maladies and found an outlet in many forms of art to help in managing their symptoms.

The military has used therapeutic arts programs since the inception of the National Intrepid Center of Excellence healing arts program in 2010 at Walter Reed National Medical Center in Bethesda, Maryland. It’s an expanding program across the nation’s military facilities, with numerous such programs in place or under way.

Signature Wounds

“One of lessons we took away from 15 years of war … is we realized there’s much more than fixing a person’s physical ability and injury,” Bono pointed out. And often, coping with such disorders with art therapy involves the community around the affected service member, she said. “l see it has a profound impact not only on your own healing, but to rest of community in terms of understanding and appreciation,” the admiral said.

Caring for a Network

“We learned we must be able to take care of the entire family and the entire network of our wounded warriors, and that was a real signature lesson we carried forward,” Bono noted.

But another piece of that equation, she said, is that military medicine learned to take care of spiritual, intellectual, mental, physical and religious domains that are important as wounded warriors transition from the military.

The DHA director told the numerous artists from the program who were in the audience that their ability to display their art in the halls of the Pentagon is an incredibly powerful way to express their messages that often cannot be put into words.

Likewise, she added, the artists’ sharing of their work with a broad audience will help others understand that complexities exist in everyone, and the complexities can exceed simple treatment and therapy.

“I want people to know who you are and what you’ve done,” Bono told the artists. “I thank you all for sharing, because I know this is a deeply personal part of who you are and what you’ve experienced.”

For more information, visit Healing Arts and the Military Health System and Pentagon Patriotic Art Program: Wounded Warrior Healing Arts Exhibit. View more photos from the opening event on Flickr and follow @WarriorCare on Twitter and Facebook for the latest in adaptive reconditioning events and updates.

By Terri Moon Cronk, DoD News, Defense Media Activity
Originally published on Defense.gov

FDA Designates Medtronic Worldwide Voluntary Field Action on HVAD(TM) System Controllers and DC Adapters as Class I Recall

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Medtronic plc (NYSE: MDT) announced today that the U.S. Food and Drug Administration (FDA) has classified the company’s recently initiated voluntary field action related to its HVAD(TM) System Controllers (serial numbers lower than CON300000) and DC Adapters (all serial numbers for product code 1435) as a Class I recall.

Medtronic began notifying clinicians outside of the United States in March 2017 about updated HVAD System Controllers and DC Adapters that were developed following two previously communicated Field Safety Notices that occurred in April 2015 and April 2016. The FDA approved the updated controller on April 7, 2017, and Medtronic began notifying U.S. clinicians about the updated HVAD Controllers and DC Adapters on April 14, 2017.

The updated controller includes enhancements designed to address the potential safety issues identified in the previously communicated notices, including:

  • strengthened power and serial port alignment guides intended to reduce the incidence of wear that could lead to damaged connector pins;
  • functionality designed to monitor internal battery performance and sound an alert when the internal battery is nearing depletion; and
  • redesigned connectors and housing intended to prevent the risk of connectors loosening or becoming more vulnerable to damage from exposure to water and other fluids.

In addition, the updated controller introduces upgraded internal circuitry designed to improve overall device reliability.

In April 2015 and April 2016, Medtronic notified clinicians about potential safety issues with the current HVAD System Controller that could lead to possible injury and death due to worn alignment guides, internal “double disconnect (no power) alarm” battery failure, and loose power and data connectors.

With the introduction of the updated controller, Medtronic has begun to remove current HVAD Controllers (product codes 1400,1401US and 1407US) in select geographies, including the U.S. Medtronic also has begun to remove the related adapters (product code 1435), Instructions for Use, Patient Manuals and Emergency Responder Guides.

As part of these activities, Medtronic has provided the following recommendations to physicians:

  • Before the updated controller will be distributed to hospitals, clinicians must complete required training on the updated controller and updated product labeling, including the Instructions for Use and Patient Manual.
  • Following training and the receipt of the updated controllers in hospital inventory, clinicians are requested to quarantine and replace patients’ primary and backup HVAD Controllers and DC adapters under clinical supervision and at a hospital where patient support equipment is available.
  • While Medtronic recommends that HVAD Controllers be exchanged, clinicians should weigh the benefits of the updated controller against the risks of a controller exchange procedure.
  • When clinicians determine a controller exchange is appropriate, they will notify patients who should promptly schedule a controller exchange as soon as the updated controllers are available.
  • Trained hospital staff must educate patients on using the updated controller.

Patients with questions about this announcement should contact their physicians or ventricular assist device (VAD) coordinator at their hospital center.

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

For information or to report a problem, please contact the 24-hour Clinical Support line at +1-888-494-6365 or email FSCA@medtronic.com.

Maintenance work begins on Forest Road 302 on Tusayan Ranger District

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TUSAYAN –A contractor working for the Kaibab National Forest began a road maintenance project this week on Forest Road 302 on the Tusayan Ranger District in order to ensure the popular route continues to meet Forest Service road standards.

The contractor is using heavy equipment to haul gravel from Dillman Pit, located about 9 miles southeast of the project location, to FR 302 where it is then being spread across the roadway to improve surface conditions. The section of FR 302 receiving this maintenance work begins at the intersection of Highway 64 south of Tusayan and continues about 5.4 miles to the intersection of FR 688.Forest Service road engineers expect the road maintenance work to continue for about five weeks and likely be complete by the end of May. While the road will not be closed during the project, motorists can expect delays and should exercise caution while traveling through the area due to varying road conditions and the presence of heavy equipment.

FR 302 is used frequently by Kaibab National Forest visitors to access camping, hunting and other recreational opportunities. Forest managers recommend using FR 688 as an alternate route during the duration of the FR 302 maintenance project in order to bypass delays and dusty conditions. Forest visitors seeking a spot for dispersed camping are also encouraged to consider other routes on the Tusayan Ranger District given the likelihood of dust and noise near the project area.

Forest Service engineers regularly evaluate and monitor road conditions across the forest to determine priorities for work. FR 302 has been in need of maintenance for some time, and forest managers expect visitors to have an improved experience once the current project is complete.

To contact the Tusayan Ranger District office, call (928) 638-2443. Additional Kaibab National Forest is available through the following sources:

  • Facebook: www.facebook.com/KaibabNF/
  • Twitter: www.twitter.com/kaibabnf (Text ‘follow kaibabnf’ to 40404 to receive text messages.)
  • Kaibab website “News & Events”: www.fs.usda.gov/kaibab