Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,348 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,348 in last 12 months

Showing 2612126140 of 46,762 recalls

DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Hydromorphone HCl 10 mg (0.2mg/ml) 50 mL syringes in 0.9% Sodium Chloride...

The Issue: Lack of Assurance of Sterility.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 9, 2017· General Mills, Inc

Recalled Item: Cascadian Farm Organic Cinnamon Raisin Granola Recalled by General Mills,...

The Issue: General Mills is recalling 2 production runs of Cascadian Farm Organic...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 6, 2017· Whole Foods Market Brand 365, Llc

Recalled Item: 365 Organic Raisin Bran Flakes 15 oz. packaged in plastic bag Recalled by...

The Issue: Undeclared (peanut) allergen: 365 Organic Peanut Butter and Cocoa Balls were...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 6, 2017· Bel Brands USA

Recalled Item: Merkts Port Wine Cheese Spread Recalled by Bel Brands USA Due to Bel Brands...

The Issue: Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2017· Kiriko, LLC.

Recalled Item: A1 Slim Recalled by Kiriko, LLC. Due to Undeclared Sibutramine

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2017· AVKARE Inc.

Recalled Item: Duloxetine Delayed-release Capsules USP Recalled by AVKARE Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: slightly elevated levels of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position...

The Issue: The base of the frame has the potential to crack when the patient is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· Allen Medical Systems

Recalled Item: Allen Medical Bow Frame Model A-70800. Surgical platform used to Recalled by...

The Issue: The base of the frame has the potential to crack when the patient is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2017· CooperSurgical, Inc.

Recalled Item: Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical...

The Issue: The 2MHZ prove was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Monteris Medical Corp

Recalled Item: MONTERIS MEDICAL NEUROBLATE SYSTEM Recalled by Monteris Medical Corp Due to...

The Issue: The firm received complaints that involved an unanticipated interaction...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2017· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...

The Issue: While reviewing documentation for the next software release of the 2008T, an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...

The Issue: Firewall installed with Philips IntelliVue Information Center iX or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 5, 2017· Purdue Pharma, LP

Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...

The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2017· Teleflex Medical

Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...

The Issue: The product has a non-conformity that may cause clips to mislead, jam or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 3, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Famotodine has an out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 3, 2017· Becton Dickinson & Co.

Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling

The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2017· Edwards Lifesciences, LLC

Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...

The Issue: Pre-procedural issues related to software defects

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...

The Issue: The table may become unstable if the nuts on the bolts were not adequately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...

The Issue: The table may become unstable if the nuts on the bolts were not adequately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 2, 2017· Unichem Pharmaceuticals Usa Inc

Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund