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 861–880 of 27,254 recalls
Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to Product service...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Instrument Recalled by Becton Dickinson & Co. Due to Product...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxFLEX Flow Cytometer Catalog Number C78500 UDI-DI code: 15099590754013 The...
The Issue: Due to a software error code that crashes during acquisition on patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assay: IMMULITE 2000 Intact PTH Recalled by Siemens Healthcare Diagnostics,...
The Issue: The potential for falsely depressed Intact PTH patient results at the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virata Preassembled Polyaxial Screw Recalled by Orthofix U.S. LLC Due to...
The Issue: Polyaxial screws do not meet performance standards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500i Clinical Analyzer Modules Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number:...
The Issue: Complaint identified issue with AI surgical planning software that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Recalled...
The Issue: Software issue for hq analyzer results in system not visibly applying...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Recalled...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump"...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Recalled...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine Pad-Pak Recalled by HeartSine Technologies Ltd Due to Due to...
The Issue: Due to customer complaints, defibrillator pads may contain damage pins that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Recalled...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7....
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7....
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airvo 2 Recalled by Fisher & Paykel Healthcare, Ltd. Due to When...
The Issue: When unintentionally disconnected from power source, humidifier device (used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P10 series with software version R4.5.7 Model Number 5877534 Recalled...
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.