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. 2,656 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,656 in last 12 months

Showing 481500 of 27,451 recalls

Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic Recalled by...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and Recalled...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Inner Sheath Recalled by Olympus Corporation of the...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and Recalled...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Medline Industries, LP

Recalled Item: DEXLOCK Achilles Repair Implant Kits Recalled by Medline Industries, LP Due...

The Issue: There have been multiple complaints of drill bit fusing to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Sheath Recalled by Olympus Corporation of the Americas Due to...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...

The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2025· Beckman Coulter, Inc.

Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Due to specific...

The Issue: Due to specific lots of diluents contributing to elevated platelet Daily...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2025· Beckman Coulter, Inc.

Recalled Item: Access 2 Reaction Vessels Recalled by Beckman Coulter, Inc. Due to It has...

The Issue: It has been determined that certain lots of Access 2 Reaction Vessels may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing