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. 2,656 recalls have been distributed to District of Columbia in the last 12 months.
Showing 901–920 of 47,654 recalls
Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: X8...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM50...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: My Bladder Recalled by Water Pure, Inc. Due to Potential E. coli Contamination
The Issue: Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Deli Express BBQ Pulled Pork on a sesame bun. Net Recalled by E.A. Sween Co....
The Issue: Potential foreign material (plastic)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lanthanum Carbonate chewable tablets Recalled by Cipla USA, Inc. Due to...
The Issue: Failed stability specifications: Out of specification for hardness test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lanthanum Carbonate chewable tablets Recalled by Cipla USA, Inc. Due to...
The Issue: Failed stability specifications: Out of specification for hardness test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAMMOMAT Inspiration Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There were instances where the operator table was sold together with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMMOMAT Fusion Recalled by Siemens Medical Solutions USA, Inc Due to There...
The Issue: There were instances where the operator table was sold together with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There were instances where the operator table was sold together with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bromocriptine Mesylate Capsules Recalled by Zydus Pharmaceuticals (USA) Inc...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardiosave Rescue Recalled by Datascope Corp. Due to The IFU addendum...
The Issue: The IFU addendum updates the Vibration and Shock Table to the correct standards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Recalled by Datascope Corp. Due to The IFU addendum...
The Issue: The IFU addendum updates the Vibration and Shock Table to the correct standards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Kiestra" Isolate Suspension Cuvette Array Recalled by Becton Dickinson &...
The Issue: The 2D barcodes on these cuvettes contain formatting errors that prevent the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...
The Issue: Firm is initiating a removal due to continued reports of adverse events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.