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. 2,353 recalls have been distributed to Alaska in the last 12 months.
Showing 22761–22780 of 27,254 recalls
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is...
The Issue: CareFusion has identified a potential for damage to the power connector on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rejuvenator Chamber manufactured by Baro-Therapies Recalled by...
The Issue: The firm is distributing the Rejuvenator device without an approved 510(k).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System PS Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA" The Personalized Knee System UC Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Posterior Stabilized Tibial...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....
The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...
The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.