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. 2,565 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,565 in last 12 months

Showing 1556115580 of 47,654 recalls

Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Troponin I STAT Immunoassay: Catalog# 05094798160 - Product Usage:...

The Issue: Recall reason is possible sporadic false negative conventional troponin...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Troponin I Immunoassay: Catalog# 05094810160 - Product Usage:...

The Issue: Recall reason is possible sporadic false negative conventional troponin...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cobalt HF Quad MRI SureScan Implantable Cardioverter Defibrillators with...

The Issue: The device may contain a manufacturing defect of a missing resistance spot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
DrugApril 6, 2021· Hyobin LLC

Recalled Item: PremierZen Black 5000 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund