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. 2,423 recalls have been distributed to District of Columbia in the last 12 months.
Showing 36621–36640 of 47,654 recalls
Recalled Item: Alkaline Wash Recalled by Abbott Laboratories Due to The product is leaking...
The Issue: The product is leaking from the cap and crystallization was noted as present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 220-230V Recalled by...
The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zebeta¿ (bisoprolol fumarate) Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Dissolution Specifications: OOS result during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0210-312-000-Woundcare Replacement kit with soft tip Recalled by Stryker...
The Issue: Potential sterility breach in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon Fast Absorbing Plain Gut - MultiPass Needles Recalled by Ethicon,...
The Issue: Ethicon Fast Absorbing Surgical Gut (Plain) Suture is being recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...
The Issue: Potential lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...
The Issue: Potential lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaySearch RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: RaySearch Laboratories AB became aware of an issue with the dose calculation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...
The Issue: Reports where patients who recently switched from the current Shiley...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...
The Issue: Reports where patients who recently switched from the current Shiley...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 250cc White Plastic Container containing 120 capsules Recalled by Natural...
The Issue: Natural Creations announces allergy alert and voluntary recall of New...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DASANI Purified Water Recalled by World of Coca-Cola Due to There is the...
The Issue: There is the potential that some of the bottles may contain linear pieces of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HDL-Cholesterol gen.3. For the quantitative determination of high-density...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglycerides/Glycerol Blanked. In vitro test for the quantitative...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXPRESS Dry Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uric Acid plus ver.2 In vitro test for the quantitative Recalled by Roche...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.