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. 2,311 recalls have been distributed to Alaska in the last 12 months.
Showing 36841–36860 of 46,762 recalls
Recalled Item: Catalys Precision Laser System-Catalys - U - US product Recalled by...
The Issue: Software anomaly on OptiMedica CATALYS System version 3.00.05 that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K2 with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008T with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008Kathome - 190895 2008T GEN 2 Recalled...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Abbott Medical Optics,...
The Issue: Device may experience loss of suction during treatment resulting in scoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY Recalled by...
The Issue: Failures of the 4.8mm of the GAP Endo-Exo Medullary System have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...
The Issue: The recalling firm was notified by the contract manufacturer that they had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caviwave Pro Ultrasonic Cleaning System Recalled by Steris Corporation Due...
The Issue: Should the Caviwave Pro Ultrasonic Cleaning System experience a temporary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers Recalled by Steris Corporation Due...
The Issue: STERIS has identified that the control board software in select AMSCO 400...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Lack of Assurance of Sterility; due to leaking vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Lack of Assurance of Sterility; due to leaking vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Spirit TM Select bed is a Med-Surg bed intended Recalled by CHG Hospital...
The Issue: It was identified that in some situations the bed exit alarm may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velocity" Biopsy Valve Recalled by US Endoscopy Group Inc Due to The company...
The Issue: The company has received reports of structural non conformance at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Connector with Suction Port Connector Recalled by King Systems...
The Issue: Product is mislabeled as Double Swivel Connector with Suction Port and is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Hemodialysis Monitor Recalled by Transonic Systems Inc Due to...
The Issue: Customer unable to obtain measurements due to the device seeing no flow or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thumb Screw for the Synthes Recon Locking Aiming Arm for Recalled by...
The Issue: For certain lots, the incorrect raw material of annealed 17-4PH Stainless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate Inj. Recalled by West-Ward Pharmaceutical Corporation Due...
The Issue: Failed Impurities/Degradation Specifications; 12 month stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breyers¿ No Sugar Added Salted Caramel Swirl 1.5-quart (1.41L) packaged...
The Issue: Unilever United States, Inc. is voluntarily recalling a limited number of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AMLODIPINE BESYLATE TABLETS USP Recalled by Qualitest Pharmaceuticals Due to...
The Issue: Failed tablet specifications: One lot was found to contain oversized tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.