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. 2,487 recalls have been distributed to Alaska in the last 12 months.
Showing 11481–11500 of 27,254 recalls
Recalled Item: Biomet 6.5 Cannulated Screw Tap - Bone fixation screw Recalled by Biomet Due...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended Recalled by...
The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Recalled by...
The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOL3650 Simplexa VZV Direct - Product Usage: is intended for Recalled by...
The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Type S Extension For use with Varian Recalled by Med Tec Inc Due to...
The Issue: Potential for disengagement of the Varian Style Type-S Extension during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL80-FLEX CO-OX 393-841 Box Label Recalled by Radiometer Medical ApS Due to...
The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL80-FLEX-393-839 Box Label Recalled by Radiometer Medical ApS Due to...
The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product Performance Verifier I Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product Performance Verifier II Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...
The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...
The Issue: The product is being recalled due to the central screw drill seizing inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...
The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Merge Application Server Software Release and Merge...
The Issue: An error in the calculation of the Michigan Ranges can generate an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Compression Screw Recalled by Stryker GmbH Due to Seal integrity of...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S Recalled by...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...
The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.