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. 2,655 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3461–3480 of 47,654 recalls
Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...
The Issue: There is an issue with the ventilator battery charger that could lead to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...
The Issue: There is an issue with the ventilator battery charger that could lead to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methadone Hydrochloride Tablets Recalled by West-Ward Columbus Inc Due to...
The Issue: Failed Tablet/Capsule Specifications: Illegible product identification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ketamine inj 50 mg per 1 mL Recalled by Hikma Injectables USA Inc Due to...
The Issue: Lack of Assurance of Sterility: The tamper-evident seal on several of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: phenylephrine in 0.9% Sodium Chloride Inj Recalled by Hikma Injectables USA...
The Issue: Lack of Assurance of Sterility: The tamper-evident seal on several of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each) Recalled by...
The Issue: During the assembly of the cartridge to its connecting body part, the valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each) Recalled by...
The Issue: During the assembly of the cartridge to its connecting body part, the valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.