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. 2,639 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3721–3740 of 47,654 recalls
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT Recalled by...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) Port Access Kit Recalled by MEDLINE...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 6 Plus Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT and Spectral CT Plus. Model Numbers: 728333 Recalled by Philips...
The Issue: Potential for a plan box not updated issue during Interventional procedure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impossible Spicy Ground Sausage Meat from plants 14oz chub Recalled by...
The Issue: product may contain pieces of metal
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Impossible Savory Ground Sausage Meat from plants 14oz chub Recalled by...
The Issue: product may contain pieces of metal
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lisinopril Tablets Recalled by Evaric Pharmaceuticals Inc. Due to Foreign...
The Issue: Presence of Foreign Object: A pharmacist discovered a metal fragment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: mint Lesion Recalled by Mint Medical GmbH Due to Some software versions have...
The Issue: Some software versions have a malfunction where they may show incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: mint Lesion Recalled by Mint Medical GmbH Due to Some software versions have...
The Issue: Some software versions have a malfunction where they may show incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gelato Recalled by Keystone Industries Due to CGMP deviations: the bulk...
The Issue: CGMP deviations: the bulk product was rejected by the Quality Unit after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Henry Schein Recalled by Keystone Industries Due to CGMP deviations: the...
The Issue: CGMP deviations: the bulk product was rejected by the Quality Unit after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quala Dental Products Recalled by Keystone Industries Due to CGMP...
The Issue: CGMP deviations: the bulk product was rejected by the Quality Unit after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: safco Recalled by Keystone Industries Due to CGMP deviations: the bulk...
The Issue: CGMP deviations: the bulk product was rejected by the Quality Unit after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dental City Recalled by Keystone Industries Due to CGMP deviations: the bulk...
The Issue: CGMP deviations: the bulk product was rejected by the Quality Unit after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.