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. 896 recalls have been distributed to Alaska in the last 12 months.
Showing 43081–43100 of 46,762 recalls
Recalled Item: BC Hammock Mesh Sling (Small) Recalled by Prism Medical Services USA Due to...
The Issue: The product does not meet the firm's size standards, the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-850-100 T5 zipper Toga with Peel Away Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sovereign¿ Compact Phacoemulsification System Recalled by Abbott Medical...
The Issue: Abbott Medical Optics Inc. (AMO) initiated this Urgent Notice of Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-820-000 T4 Zipper Toga (L/XL) Sterile Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BC Hammock Mesh Sling (Medium) Recalled by Prism Medical Services USA Due to...
The Issue: The product does not meet the firm's size standards, the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-760-000 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-830-000 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments0400-750-000 T4 Toga Recalled by Stryker Instruments Div....
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-710-000 T4 Pullover Toga (S/M) Sterile Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-850-000S2 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-820-000S3 T4 Toga w/Inside Shoulder Ties Recalled...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mother Earth Products Recalled by Mother Earth International LLC Due to...
The Issue: The product was manufactured with a Soy Protein Isolate manufactured by CHS,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monaco RTP System Radiation Therapy Treatment Planning System. Radiation...
The Issue: Patient needs to be positioned as indicated by the treatment plan.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to leaking pouches
The Issue: leaking pouches
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride and 5% Dextrose Injection Recalled by Baxter...
The Issue: Lack of Assurance of Sterilty: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zolpidem Tartrate Tablets 5 mg Recalled by American Health Packaging Due to...
The Issue: Unit Dose Mispackaging: This recall event is due to a random undetected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nimodipine Capsules 30 mg Recalled by Sun Pharmaceutical Industries Inc. Due...
The Issue: Crystallization; crystallized nimodipine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Folic Acid Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.