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. 2,429 recalls have been distributed to District of Columbia in the last 12 months.
Showing 35861–35880 of 47,654 recalls
Recalled Item: Italian Blend. Product is IQF frozen Recalled by National Frozen Foods...
The Issue: Italian Blend product is recalled due to potential to be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Frozen Sliced Saku Tuna Product of Indonesia. The bulk Recalled by Osamu...
The Issue: Osamu Corporation is recalling frozen chunk, ground, sliced saku, saku, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Frozen Ground Tuna Product of Indonesia. The bulk frozen Recalled by...
The Issue: Osamu Corporation is recalling frozen chunk, ground, sliced saku, saku, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Frozen Tuna Loin Product of Indonesia. The bulk frozen Recalled by Osamu...
The Issue: Osamu Corporation is recalling frozen chunk, ground, sliced saku, saku, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Frozen Saku Tuna Product of Indonesia. The bulk frozen Recalled by Osamu...
The Issue: Osamu Corporation is recalling frozen chunk, ground, sliced saku, saku, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Frozen Tuna Chunks Product of Indonesia. The bulk frozen Recalled by...
The Issue: Osamu Corporation is recalling frozen chunk, ground, sliced saku, saku, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: cobas b 123 Fluid Pack COOX 200 Product Recalled by Roche Diagnostics...
The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 123 Fluid Pack COOX 400 Product Recalled by Roche Diagnostics...
The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phentermine Hydrochloride Capsules Recalled by KVK-Tech, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Intermezzo (zolpidem tartrate) Recalled by Purdue Pharma L.P. Due to Failed...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mometasone Furoate Ointment USP Recalled by Perrigo Israel Pharmaceuticals...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Akttive High Performance Fat Burner Gold dietary supplement capsules...
The Issue: Marketed Without An Approved NDA/ANDA: Dietary supplements contains...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....
The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS500 of an IACS Workstation Critical Care (Evita Infinity V500) Recalled by...
The Issue: The battery capacity of the optional PS500 of an IACS Workstation Critical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray....
The Issue: Electrostatic energy may be stored in Systems that can cause a short-cicuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....
The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etac Relax wall mounted shower seat The Etac Relax is Recalled by Etac...
The Issue: The recalling firm has received reports of a malfunction of the Relax wall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A gradient cable in the ACGD...
The Issue: A gradient cable in the ACGD cabinet may be missing a spacer that prevents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery Recalled by...
The Issue: Stryker Sustainability Solutions has received reports indicating that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfectum Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.