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. 2,629 recalls have been distributed to District of Columbia in the last 12 months.
Showing 5561–5580 of 27,451 recalls
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CellQuicken Analyzer (Smart-Watch and Software) Recalled by RoyalVibe Health...
The Issue: Ultrasound devices were not authorized, cleared, or approved by FDA, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citrine Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4500MD Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API3200MD Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citrine QTRAP Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box as labeled: Regard Recalled by CooperSurgical, Inc. Due to Incorrect...
The Issue: Incorrect component descriptions within the "Contents" section on the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to...
The Issue: Device is breaking while in use, potential for patients to require a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to There is...
The Issue: There is the potential that the safety shield may not properly engage on IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem P Recalled by TECHNO-PATH MANUFACTURING LTD. Due to Technopath...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem S Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM Recalled by...
The Issue: Peripheral coil system detachable has a potential of unsealed pouch packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Medical Products stored on pallets Recalled by Inmar Supply Chain...
The Issue: Various medical devices potentially exposed to rodent and rodent activity....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.