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.
Showing 26801–26820 of 46,762 recalls
Recalled Item: Argatroban Injection Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...
The Issue: Lack of Assurance of Sterility: Customer complaints for leaking bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corporation Due to Lack...
The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corporation Due...
The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product...
The Issue: The diameter of the Fogarty Catheter balloon, measures 6mm instead of 10mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-ZINE Rapid Size and Strength capsules Recalled by HARDCORE FORMULATIONS...
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA-STEN Rapid Size and Strength capsules Recalled by HARDCORE...
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clif Builders Chocolate Mint 12-count Recalled by Clif Bar & Company Due to...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Kid Zbar Protein Chocolate Chip 10-pack Recalled by Clif Bar & Company...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Kid Zbar Protein Chocolate Mint 10-pack Recalled by Clif Bar & Company...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Builders Variety Pack Chocolate Peanut Butter and Chocolate Mint...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Kid Zbar Protein Variety Pack 30-count Recalled by Clif Bar & Company...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Anarkali Peshawari Naan Bread Frozen 15oz. retail plastic pouch 24 Recalled...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...
The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number:...
The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche / Hitachi MODULAR Analyzer Systems-Immunoassay...
The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia 1000 Instrument Recalled by Phadia US Inc Due to The "Retry" command...
The Issue: The "Retry" command does not function properly which could cause a shortage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product...
The Issue: A small number of batches may crack or break if exposed to certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600...
The Issue: Teleflex Medical is recalling the affected product because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...
The Issue: Replacement campaign on all units that have a gas spring head in aluminum.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.