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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,542 in last 12 months

Showing 1660116620 of 27,451 recalls

Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Merge Healthcare, Inc.

Recalled Item: Merge Unity software Recalled by Merge Healthcare, Inc. Due to The software...

The Issue: The software is not identifying the patient as having atypical hyperplasia,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Spectranetics Corporation

Recalled Item: Spectranetics Bridge Occlusion Balloon catheter Recalled by Spectranetics...

The Issue: Possible inability to pass the guidewire through the Bridge device,...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2017· Mako Surgical Corporation

Recalled Item: Total Hip Application (THA) Product Usage: The Robotic Arm Interactive...

The Issue: Software discrepancy of not showing all the EE constants, when the screen is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing