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. 2,550 recalls have been distributed to Alaska in the last 12 months.
Showing 2341–2360 of 46,762 recalls
Recalled Item: Catalog No. 8888160341 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pre-filled Water Syringe Recalled by Healthmark Industries Co., Inc. Due to...
The Issue: During endoscope surveillance monitoring, a user facility identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160119 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160325 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160333 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160648 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160556 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...
The Issue: Firm has identified Drug Library Management defects in the software: 1) DLM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Drill Stop Kit is the version of the Mini Recalled by Implant Direct...
The Issue: The Drill stop kit contains incorrect components.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth...
The Issue: Product may have an off color affecting perfomance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Manual Resuscitator with Medium Adult Mask Recalled by SunMed...
The Issue: Affected lots were manufactured with B/V Filter incorrectly attached to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...
The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...
The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rodex Forte Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...
The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prothin Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...
The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Probese Caps Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...
The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Super ProTHIN Plus Recalled by Preventics, Inc. dba Legere Pharmaceuticals...
The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NutriLean Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...
The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protrim Plus Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...
The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...
The Issue: A manufacturing defect in the sample probe (S probe). The corners of the tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.