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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18981–19000 of 27,451 recalls
Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: Recalled by...
The Issue: Sterility compromised due to breach in sterile packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva with Flat Detector Recalled by Philips Electronics North...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOMAD Pro2 Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...
The Issue: Firm received customer complaints where end users reported that Nomad Pro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOMAD Pro Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...
The Issue: Firm received customer complaints where end users reported that Nomad Pro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy Cranial S7. The software application is sent in CD format with an...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...
The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FrameLink. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy Spine. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-450BR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 501 Post-Analytical Unit calculator/data processing module Recalled...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche/Hitachi MODULAR Analytics Combination Systems Modular D/P: Clinical...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 471 centrifuge unit calculator/data processing module Recalled by...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 701 Post-Analytical Unit calculator/data processing module Recalled...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.