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. 2,622 recalls have been distributed to District of Columbia in the last 12 months.
Showing 6681–6700 of 27,451 recalls
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM Recalled by...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES AUX Tower BD Pyxis Recalled by CareFusion 303, Inc....
The Issue: Due to an increase in complaints of door latch assembly failures that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KLS martin Group KLS E-COUPLING ADAPTER E-Coupling Adapter Recalled by...
The Issue: Incorrect Unique Device Identifier/GTIN code was used on product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edward Lifesciences Recalled by Edwards Lifesciences, LLC Due to There is a...
The Issue: There is a potential that the distal end of the catheter may be bent beyond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edward Lifesciences Recalled by Edwards Lifesciences, LLC Due to There is a...
The Issue: There is a potential that the distal end of the catheter may be bent beyond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on...
The Issue: A component of a sub-assembly used in the affected AEDs had not undergone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clariti 1-day toric soft contact lenses Recalled by CooperVision, Inc. Due...
The Issue: The lenses manufactured in the affected lot were made with a misaligned axis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Anesthesia ES System (PAS ES) Recalled by CareFusion 303, Inc. Due...
The Issue: Automated dispensing cabinet drawer firmware may have inadvertently been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brainlab ExacTrac Dynamic software Recalled by Brainlab AG Due to Deep...
The Issue: Deep Inspiration Breath Hold (DIBH) functionality may not work as specified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus Exchange Kit Therapeutics. Component of Amicus Separator...
The Issue: Potential for centrifuge packs to develop a stress leak for certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus MNC Apheresis Kit Double Needle. Component of Amicus Separator...
The Issue: Potential for centrifuge packs to develop a stress leak for certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Global Total LP single step medium Recalled by CooperSurgical, Inc. Due to...
The Issue: It has come to CooperSurgical's attention that the affected Product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to Firm has...
The Issue: Firm has initiated a removal of the product due to insufficient evidence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.