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. 2,547 recalls have been distributed to District of Columbia in the last 12 months.
Showing 15541–15560 of 27,451 recalls
Recalled Item: Fortify Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadra Assura MP Recalled by St Jude Medical Inc. Due to The firm is...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor Recalled by St Jude...
The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promote Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model...
The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Current Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promote Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS programmer (Model # 3650) Recalled by St Jude Medical Inc. Due to...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...
The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Recalled by CareFusion 303, Inc. Due to The bezel manufacturing...
The Issue: The bezel manufacturing process for the FR-110 plastic may have resulted in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to The pumps may switch to...
The Issue: The pumps may switch to stand-by during use requiring the pump to be reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Certain Barrel Clamp Guides may contain a ridge that could potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.