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. 2,660 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,660 in last 12 months

Showing 4160 of 27,451 recalls

Medical DeviceJanuary 21, 2026· Physio-Control, Inc.

Recalled Item: PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog...

The Issue: Due to pediatric defibrillator electrode delamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Agiliti Health - Ellis

Recalled Item: Adapt Pump Recalled by Agiliti Health - Ellis Due to Agiliti identified an...

The Issue: Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Stryker Corporation

Recalled Item: MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm...

The Issue: Due to a need to update the product labeling (Instructions for Use IFU) as a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Roche Diagnostics Operations, Inc.

Recalled Item: cobas pro integrated solutions with cobas c 503 analytical units: Recalled...

The Issue: Software defect, which allows the system to accept erroneous, non-monotonous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing