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. 1,057 recalls have been distributed to Alaska in the last 12 months.
Showing 8541–8560 of 46,762 recalls
Recalled Item: QUADROX-iD Pediatric Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HMOD 70000-USA/QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro...
The Issue: May not meet the stability specifications for shelf life outlined in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HMOD70000-USA/QUADROX-iD Recalled by Maquet Medical Systems USA Due to...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to 1. An accessory may...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glycopyrrolate Tablets Recalled by Aurolife Pharma, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hu Vanilla Crunch Dark Chocolate bar Recalled by HU PRODUCTS Due to...
The Issue: may contain undeclared tree-nuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech...
The Issue: Medtronic has identified that the logfiles downloaded from the recently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale...
The Issue: The Resuscitaire Infant Radiant Warmer with the optional scale could display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeris Balloon Dilation Catheter Recalled by Bryan Medical Inc Due to Mislabeling
The Issue: Devices were mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation Storage and Retrieval Module (SRM) Recalled by Siemens...
The Issue: A firmware error may lead to an incorrect association of test result(s) to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite Systems with 9-inch Image Intensifier Recalled by GE OEC Medical...
The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Flexiview 8800 Systems with 9-inch Image Intensifier Recalled by GE OEC...
The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.