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. 2,550 recalls have been distributed to Alaska in the last 12 months.
Showing 3081–3100 of 27,254 recalls
Recalled Item: Olympus Gastrointestinal Videoscope Recalled by Olympus Corporation of the...
The Issue: It was discovered during device performance testing that the CCD imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...
The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...
The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemo. Versions 14.2 Recalled by CHANGE...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci 5 Recalled by Intuitive Surgical, Inc. Due to Surgical system Error...
The Issue: Surgical system Error 23062 due to connector1) Partially damaged "Potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo. Version 12.2. Recalled by CHANGE HEALTHCARE CANADA...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortera Spinal Fixation System Screw Recalled by XTANT Medical Holdings, Inc...
The Issue: Spinal fixation system implant screws marked "DNI" are not intended to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BinaxNOW Respiratory Strep A Test Kit Recalled by Cypress Medical Products...
The Issue: Due to a classification error in our inventory management system, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acceava Respiratory Strep A Recalled by Cypress Medical Products LLC Due to...
The Issue: Due to a classification error in our inventory management system, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miami J Select Collar Recalled by Ossur H / F Due to Pressure sensitive...
The Issue: Pressure sensitive adhesive hooks attached to the sides of the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixSKY Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BlueFIRE Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StabiliT TOUCH Syringe Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiamondTOUCH Digital Inflation Device Recalled by Merit Medical Systems,...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Inflation Kit Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSystem Inflation Device Recalled by Merit Medical Systems, Inc. Due...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.