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. 1,056 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
1,056 in last 12 months

Showing 2481–2500 of 27,451 recalls

Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· 3M Company - Health Care Business

Recalled Item: Clarity Precision Grip Attachments Recalled by 3M Company - Health Care...

The Issue: Attachments may not mate with the tooth as intended in the digital treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) CRANI Recalled by...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· Abbott Medical

Recalled Item: The Merlin PCS 3650 programmer Model 3330 The Merlin PCS Recalled by Abbott...

The Issue: Due to a programmer software anomaly, during finalizing of the leadless...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) FREE FLAP Recalled by...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· GE OEC Medical Systems, Inc

Recalled Item: OEC 3D Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc Due...

The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· GE OEC Medical Systems, Inc

Recalled Item: OEC Elite Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...

The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· Medtronic Neuromodulation

Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...

The Issue: Software issues were identified in application version 2.x.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· GE OEC Medical Systems, Inc

Recalled Item: OEC 9900 Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...

The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing