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. 2,480 recalls have been distributed to Alaska in the last 12 months.
Showing 14101–14120 of 27,254 recalls
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit Recalled by Westmed, Inc. Due...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask Recalled by...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask Recalled by...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proximal Humerus Plate Recalled by Miami Device Solutions, LLC. Due to Right...
The Issue: Right Proximal Humerus Plates. Product component parts MDS130108R, may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Burr Recalled by Arthrex, Inc. Due to Devices may generate excessive...
The Issue: Devices may generate excessive heat during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Urinary Drainage bag Recalled by Teleflex Medical Due to The device...
The Issue: The device labels are not UDI compliant. The missing UDI compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIMADZU MobileDaRt Evolution (MX8 Version) Recalled by Shimadzu Medical...
The Issue: In these units, the brake is usually released by gripping the drive handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH CARE Premium Drain bag Recalled by Teleflex Medical Due to The device...
The Issue: The device labels are not UDI compliant. The missing UDI compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use Recalled by...
The Issue: False negative results with the BD MAX Extended Enteric Bacterial Panel when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is...
The Issue: Normal operation of the device is to power up the device in the morning,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: aap Implante AG Recalled by AAP Implantate Ag Due to There is the potential...
The Issue: There is the potential for the Lambotte chisel to break at the welded piece...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethyl Alcohol Enzymatic Assay Recalled by Lin-Zhi International Inc Due to...
The Issue: Shelf life of the product may be reduced due to degradation of the assay.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 21Y15 MagValve Product Usage: The PushValves/ MagValves is intended...
The Issue: Some of the installed valve-inserts have a diameter smaller than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...
The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...
The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 21Y14 PushValve Product Usage: The PushValves/ MagValves is intended...
The Issue: Some of the installed valve-inserts have a diameter smaller than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is...
The Issue: Some of the installed valve-inserts have a diameter smaller than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management...
The Issue: User-induced circumstances can contribute to the EVOLIS Microplate Processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...
The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.