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. 2,251 recalls have been distributed to Alaska in the last 12 months.
Showing 44141–44160 of 46,762 recalls
Recalled Item: Lansoprazole Delayed-release Capsules Recalled by Mylan Pharmaceuticals Inc....
The Issue: Presence of Foreign Tablets/Capsules: Bottles of lansoprazole 30 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Z Pro 25 High Protein Supplement Net. Wt. 1.5 oz. Recalled by R-Kane...
The Issue: Z Pro High Protein Chocolate Flavor Supplement is under recall since it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Z Pro 25 High Protein Supplement Net. Wt. 1.3 oz. Recalled by R-Kane...
The Issue: Z Pro High Protein Vanilla Flavor Supplement is under recall because it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Vascular...
The Issue: Vascular Solutions, Inc has discovered a potential problem with a number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The...
The Issue: Philips HeartStart XL+ Defibrillator/Monitor may become locked out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian Eclipse Treatment Planning System for Radiotherapy Recalled by Varian...
The Issue: The calculation of dose dynamic plans containing different energy fields is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...
The Issue: Some devices had broken through the seal of the sterile pouch. ConMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE HYFRECATOR(R) ELECTRODES - SHARP Recalled by ConMed Corporation...
The Issue: Some devices had broken through the seal of the sterile pouch. ConMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bacterin Elutia Recalled by Bacterin International, Inc. Due to A portion of...
The Issue: A portion of a silicone wound drain was found to be cracked.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isoline Implantable Defibrillation Lead Recalled by Sorin Group USA, Inc....
The Issue: Isoline defibrillation leads distributed may have internal insulation breach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical C-Series Carry Bar Recalled by Prism Medical Services USA Due...
The Issue: The firm replaced the recalled carry bar with a plastic insert with a carry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 700 Series Ventilators (PB740 and PB760) PB700 Series...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proplege Coronary Sinus Catheter model PR9 Recalled by Edwards Lifesciences,...
The Issue: Edwards Lifesciences is recalling certain Proplege Coronary Sinus Catheter,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY TINGLING JELLY Personal Lubricant. The product is packaged into Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Non-Sterility: Confirmed customer complaint of product contaminated with mold.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...
The Issue: Firm was made aware of incidents relating to the difficulty of properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.