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 26281–26300 of 27,451 recalls
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hem-o-lok Large Polymer Ligating Clips Recalled by Teleflex Medical Due to...
The Issue: Product is being recalled due to the possibility that the tray may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Belmont Rapid Infuser Recalled by Belmont Instrument Corporation Due to Leak...
The Issue: Leak from a saline bag caused saline to drip along the back of the Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ILLlCO¿ MIS Posterior Fixation System Recalled by Alphatec Spine, Inc. Due...
The Issue: The firm initiated the recall because the stainless steel guide-wire of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module System 9000 The Sarns Centrifugal...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Oncology...
The Issue: An anomaly has been identified with the ARIA Oncology Information System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...
The Issue: We are notifying you of a potential interaction between therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray V12 Size: 320 mm X 320 mm X 450 Recalled by Mindray DS USA, Inc....
The Issue: Mindray has identified an issue with the V Series Monitor where the monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Trilogy Acetabular System Shell with Cluster Holes Porous 56 Recalled by...
The Issue: Zimmer Trilogy¿ Acetabular System Shell with Cluster Holes, Porous,56 MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.