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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 26141–26160 of 27,451 recalls
Recalled Item: OmniGuide BP-ROBOTIC ( BeamPath Robotic) Recalled by OmniGuide, Inc. Due to...
The Issue: Failure of glue joint, allowed a portion of the single use device to shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparoscope Recalled by Applied Medical Resources Corp Due to Applied...
The Issue: Applied Medical is conducting a voluntary recall on a specific lot number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access hLH assay is a paramagnetic particle Recalled by Beckman Coulter...
The Issue: Beckman Coulter Inc. (BEC) has demonstrated that real time stability testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Composite Series Base Unit Recalled by Integra LifeSciences...
The Issue: An investigation of an adverse trend of complaints conducted by Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Composite Series Skull Clamps Recalled by Integra LifeSciences...
The Issue: An investigation of an adverse trend of complaints conducted by Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators are...
The Issue: The BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Trauma Nail System. The devices are indication for bone fixation....
The Issue: Recall was initiated due to the possibility that the outer pouch was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brookstone Heated Body Bean Recalled by Brookstone Company, Inc. Due to...
The Issue: Additional Warning Statement to prevent burns to the skin
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Modular Humeral Head 48mm x 24mm Ti 6AI4V/Ion Implanted (Orthopedic...
The Issue: The items in this lot are missing the ion implantation feature. The surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B...
The Issue: Ortho Clinical Diagnostics is recalling certain lots of the Vitros Anti-HBs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.