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. 2,374 recalls have been distributed to Alaska in the last 12 months.
Showing 20801–20820 of 27,254 recalls
Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...
The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N:...
The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...
The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (100) tests Part...
The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (250) tests Part...
The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Flexi-slip tracheal tube Stylet Recalled by Teleflex Medical Due to...
The Issue: Due to reports of the plastic coating of the stylet splitting and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Mislabeling
The Issue: Sterilmed, Inc. is recalling its reprocessed Zimmer Tourniquet Cuff, Part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180 Recalled by Olympus...
The Issue: Insufficient information for specific cleaning accessories used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monode Recalled by DJO, LLC Due to Overheating and burning of the wire...
The Issue: Overheating and burning of the wire insulation inside the applicator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aliquot Delivery Kit (Syringe and Plunger) Recalled by Orthovita, Inc., dBA...
The Issue: Two isolated instances of holes in the outer header bag component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System with software versions VB10B and lower...
The Issue: The ACUSON SC2000 ultrasound system considers uppercase/lowercase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Physio-Control QuikCombo Pacing/Defibrillation/ECG Electrodes RediPak¿...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediTrace Cadence Adult Zoll Recalled by Covidien LLC Due to Multi-Function...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIVATORS HEMOCOR HPH700 Recalled by Medtronic Perfusion Systems Due to...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid...
The Issue: Some devices exhibit backup VVI operation due to a backup reset.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PenBlade Safety Scalpel Recalled by Zien Medical Technologies, Inc Due to...
The Issue: Cracks were discovered in the PET tray of a small population of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC PERFUSION TUBING PACKS (with potentially affected...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Marker Spheres The Disposable Marker Spheres used Recalled by...
The Issue: Disposable Marker Spheres (DRMS) for Brainlab Image Guided Surgery (IGS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actifuse ABX/Actifuse MIS System A bone void filler intended only Recalled...
The Issue: Baxter Healthcare is issuing a voluntary recall for all lots of Actifuse ABX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.