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. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 26361–26380 of 27,254 recalls
Recalled Item: DePuy Custom Implant Devices Packaging: Packaging was not standardized on...
The Issue: In connection with a Warning Letter received from the U.S. Food & Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V60 Ventilator Recalled by Respironics California Inc Due to Respironics is...
The Issue: Respironics is recalling the V60 ventilator because certain blower motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R)...
The Issue: Firm has confirmed highter imprecision with the recalled lots on Beckman...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MAYFIELD¿ Horseshoe Gel Pads are used in conjunction with Recalled by...
The Issue: An investigation of customer complaints identified that for two product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multileaf Collimator To be used for single or multiple fractions Recalled by...
The Issue: Information released with the product Agility did not originally contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TxRx Knee 15 Coil 3T. For use in conjunction with Recalled by Quality...
The Issue: On July 27, 2012, it was reported to the firm that the Siemens 3T 15ch Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Bio-Rad MONOLISA Anti-HBs EIA is for In Vitro Diagnostic Recalled by...
The Issue: Prolonged exposure of the MONOLISA Anti-HBs EIA Conjugate Diluent component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MAYFIELD¿ Horseshoe Gel Pads are used in conjunction with Recalled by...
The Issue: An investigation of customer complaints identified that for two product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Cardiovascular (CV) Reporting Reporting tool used for structured...
The Issue: Content entered into the "Conclusions" free text box on the Report Writer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interface module for CDl System 100/101 Product Usage: The Interface...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Styker Orthobiologics Vita Plasma Separator Recalled by Stryker...
The Issue: When preparing plasma using VitaPrep, it was reported that a small amount of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Recalled by...
The Issue: St. Jude Medical has informed your doctor that a number of cases have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini - 3788 (IPG) Recalled by St. Jude Medical Due to As part of St....
The Issue: As part of St. Jude Medical's routine tracking and product monitoring, they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini - 3721 (Charger). Product Usage: Eon Mini system Recalled by St....
The Issue: St. Jude Medical has informed your doctor that a number of cases have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.