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. 2,373 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,373 in last 12 months

Showing 13811400 of 47,654 recalls

FoodSeptember 3, 2025· Endico Potatoes Inc

Recalled Item: Endico brand PEAS & CARROTS Recalled by Endico Potatoes Inc Due to Potential...

The Issue: Product may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 3, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Viorele Recalled by Glenmark Pharmaceuticals Inc., USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 3, 2025· Endico Potatoes Inc

Recalled Item: Endico brand MIXED VEGETABLES Recalled by Endico Potatoes Inc Due to...

The Issue: Product may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Biplane Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Kit for the Preparation of Technetium Tc 99m Mertiatide Recalled by SUN...

The Issue: Failed Dissolution Specifications-Out of Specification (OOS) observation for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Potential issue that can cause the device to register "phantom" touches in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper CV20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing