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. 2,616 recalls have been distributed to District of Columbia in the last 12 months.
Showing 7561–7580 of 27,451 recalls
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...
The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog Recalled by...
The Issue: OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Early Bird Bleed Monitoring System Introducer Sheath Set Recalled by...
The Issue: Bleed monitoring system device design error, causing the device to not power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane- Model No. 11327600 Artis icono floor- Model No....
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model Recalled by Siemens...
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno- Model No. 10849000 Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...
The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...
The Issue: Firm noted an increase in customer reports of leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: Burns of varying degrees can occur to patients with electrodes left in while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200...
The Issue: Distribution of COVID Test Kits without FDA Approval, Clearance or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LineSider Spinal System pedicle screws Recalled by Integrity Implants Inc....
The Issue: Potential for intraoperative screw head separation at weld location.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.