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. 1,027 recalls have been distributed to Alaska in the last 12 months.
Showing 14941–14960 of 46,762 recalls
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER Recalled by Roche Diagnostics...
The Issue: Roche received several complaints regarding increased control recovery and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate Injectable Suspension USP Recalled by Teva...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enoki Mushroom Product of Korea Net Wt. 200 g/7.05 oz. Recalled by GOLDEN...
The Issue: Michigan Department of Agriculture and Rural Development sampled product and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ProBP 3400 Digital Blood Pressure Device ((handheld Recalled by Welch Allyn...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Recalled by...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin Recalled by Remel Inc...
The Issue: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centaur Syphilis Assay-SYP Kit Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for the ADVIA Centaur Syphilis assay to carryover into other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 27 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrodissection Cannula (Chang) Recalled by Anodyne Surgical Due to The...
The Issue: The product may have a yellowish-brown/greenish-brown residue present at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPTAR Laser Range Finders Recalled by Potomac River Group, Corp. Due to...
The Issue: RAPTAR units are capable of being field modified to enable the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 21 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 17 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rubber Dam Clamp Recalled by Dentech Corp. Due to Removing parts for safety...
The Issue: Removing parts for safety reasons due to possible breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.