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 1661–1680 of 27,451 recalls
Recalled Item: The Drill Stop Kit is the version of the Mini Recalled by Implant Direct...
The Issue: The Drill stop kit contains incorrect components.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth...
The Issue: Product may have an off color affecting perfomance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Manual Resuscitator with Medium Adult Mask Recalled by SunMed...
The Issue: Affected lots were manufactured with B/V Filter incorrectly attached to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...
The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...
The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...
The Issue: A manufacturing defect in the sample probe (S probe). The corners of the tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...
The Issue: Sample probes with defective probe tips, when used with clinical chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5008X HDF Hemodialysis Blood Tubing Set Recalled by Fresenius Medical Care...
The Issue: Potential of blood leak occurring between the lower port of the venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to the potential that some units within specific lots were damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to the potential that some units within specific lots were damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to the potential that some units within specific lots were damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution. Catalog numbers: RFP-400 Recalled by NxStage...
The Issue: Potential for the perimeter seal on the small chamber of the two-chamber bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex AMP Kit Recalled by Abbott Molecular, Inc. Due to...
The Issue: There were reports of an increase in reactive negative controls and false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex Amplification (AMP) Kit (CE) Recalled by Abbott...
The Issue: There were reports of an increase in reactive negative controls and false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AcoSound. Model Number: LW12-BTE-M Recalled by HANGZHOU ACOSOUND TECHNOLOGY...
The Issue: Three issues 1. Label error: The manufacturer information in the labeling is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Tecfen Medical Product Name: 3.2mm Slit Knife Recalled by Tecfen...
The Issue: Sterility assurance for Ophthalmic knives.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Tecfen Medical Product Name: 2.0mm Crescent Knife Angled...
The Issue: Sterility assurance for Ophthalmic knives.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Tecfen Medical Product Name: 15 degree Stab Knife Recalled by...
The Issue: Sterility assurance for Ophthalmic knives.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Tecfen Medical Product Name: 2.8mm Slit Knife Recalled by Tecfen...
The Issue: Sterility assurance for Ophthalmic knives.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MUSE 5 Systems Recalled by GE Medical Systems Information Technologies Inc...
The Issue: The MUSE Administrator Account active directory or local credential could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.