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 9601–9620 of 46,762 recalls
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to a failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: There have been reported failures of the high pressure helium regulator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial mobile application Recalled by Securitas Healthcare LLC Due to The...
The Issue: The mobile application for Android devices downloaded from the Google Play...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA comprises AST Filters in conjunction with VITEK MS Recalled by...
The Issue: For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Alvogen, Inc Due to Sub-Potent...
The Issue: Sub-Potent Drug: Out of specification for assay at the 24 month interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abelcet (Amphotericin B Lipid Complex) Injection Recalled by Leadiant...
The Issue: Lack of assurance of sterility: Medial fill with presence of Cupriavidus...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACL ELITE PRO-Analyzer designed specifically for clinical use in the...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics Recalled by...
The Issue: Potential for product manifold to crack during use on patients, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD ACCESS Closed Suction System for Neonates/Pediatrics Recalled by...
The Issue: Potential for product manifold to crack during use on patients, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE PRO )-Analyzer designed specifically for clinical use in Recalled...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avanos Ballard Oral Care Swab Recalled by Avanos Medical, Inc. Due to...
The Issue: Incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE- Analyzer designed specifically for clinical use in the Recalled...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE designed specifically for clinical use in the Recalled by...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology,...
The Issue: Stryker has identified an issue that impacts two specific lots of CLAW" II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or a Recalled by...
The Issue: In the event of any unintended table movement, the system may not detect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology,...
The Issue: Stryker has identified an issue that impacts two specific lots of CLAW" II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or Trumpf/MAQUET...
The Issue: If, during the procedure, X-ray has been released and a image has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EndoHPB Bipolar Radiofrequency (RF) Catheter 8F (2.7mm). A...
The Issue: Cease use of the Habib EndoHPB Bipolar RF Catheter with the ERBE VIO3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.