Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,584 recalls have been distributed to District of Columbia in the last 12 months.
Showing 11521–11540 of 27,451 recalls
Recalled Item: A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE LEFT 14 HOLE 227MM...
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: 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: Atellica Solution IM1300 Analyzer Recalled by Siemens Healthcare...
The Issue: Insufficient sample may not be detected when using Tube Top Sample Cup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Solution IM1600 Analyzer Recalled by Siemens Healthcare...
The Issue: Insufficient sample may not be detected when using Tube Top Sample Cup...
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.