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.
Showing 1401–1420 of 47,654 recalls
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.
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.
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.
Recalled Item: Allura Xper FD20 Biplane Product Codes: (1)722013 Recalled by PHILIPS...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
Recalled Item: Allura Xper FD10 OR Table 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.
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.
Recalled Item: Allura Xper FD20/15 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.
Recalled Item: Allura Xper FD20 OR Table 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.
Recalled Item: Allura Xper FD10C 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.
Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: The BIOS battery may deplete faster than initially anticipated during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norgestimate and Ethinyl Estradiol Tablets Recalled by AvKARE Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616 Recalled by...
The Issue: The bovine carotid arteries used to produce the impacted grafts from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.