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. 2,480 recalls have been distributed to Alaska in the last 12 months.
Showing 15341–15360 of 46,762 recalls
Recalled Item: Admin Set w/ClaveTM Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Abre Venous Self-expanding Sent System Recalled by Medtronic Inc....
The Issue: Incorrect size printed on the device; packaging is labeled correctly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Controller - Product Usage: intended for use with a Recalled by Boston...
The Issue: May have been programmed with a less than optimal brightness setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS¿ CMV IgM 30 Tests Recalled by Biomerieux Inc Due to bioMerieux...
The Issue: bioMerieux received complaints about calibration issue observed on several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuts.com brand Diced Dried Figs packaged in 1lb stand up gusset pouches....
The Issue: Undeclared almonds in diced fig product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....
The Issue: BBMI has identified through complaints the potential for the extension set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...
The Issue: Possible false negative or false positive results due to the product being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOMA-Jet 10 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...
The Issue: Defective Delivery System: customer complaints concerning the injector pen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOMA-Jet 5 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...
The Issue: Defective Delivery System: customer complaints concerning the injector pen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Lack of Assurance of Sterility: customer complaints of loose crimped vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)...
The Issue: Failure to comply with the performance standard for fluoroscopy systems. Per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium X TL Instruments - intervertebral fusion device with bone graft...
The Issue: Stryker identified non-conforming instruments that are components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Opening Wedge Osteotomy Plate Recalled by Arthrex, Inc. Due to It was...
The Issue: It was discovered that five AR-13200ST-15.0 parts were processed as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHINA-GEL WHITE (Camphor 3.00% Recalled by China Gel Inc Due to CGMP...
The Issue: CGMP deviations: Product being recalled as it was made in the same facility...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHINA_GEL (Camphor 3.00% Recalled by China Gel Inc Due to CGMP deviations:...
The Issue: CGMP deviations: Product being recalled as it was made in the same facility...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: aulief (Organic Camphor 3.00% Organic Menthol 5.00%) Recalled by China Gel...
The Issue: CGMP deviations: Product being recalled as it was made in the same facility...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.