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 15841–15860 of 27,451 recalls
Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard(R) Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD has...
The Issue: BMD has identified that the product code/lot number combination identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard(R) Premature Infant Feeding tube Recalled by C.R. Bard, Inc. Due to BMD...
The Issue: BMD has identified that the product code/lot number combination identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System)...
The Issue: Recently Integrity Implants uncovered a discrepancy in the cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE Recalled by Radiometer Medical ApS Due to There is a potential problem...
The Issue: There is a potential problem relating to the AQURE System, versions 2.3.0...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard(R) Adult/Pediatric Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...
The Issue: BMD has identified that the product code/lot number combination identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard(R) Premature Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...
The Issue: BMD has identified that the product code/lot number combination identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sternal Valve Retractors With Atrial and Aortic Rakes Recalled by Genesee...
The Issue: Failure in a retractor blade due to corrosion. In the area of the blade...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wet-Field Hemostatic Eraser Bipolar 25G Recalled by Beaver-Visitec...
The Issue: Products were packaged with incorrect labeling,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to There is...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO lnfiniti Needle Guide Bracket. used for performing needle-guided (or...
The Issue: A cover failed leak testing during validation testing of new needle guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Zipper Toga (S/M) Recalled by Stryker Instruments Div. of Stryker...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Zipper Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Zipper Toga with Peel-Away Face Shield Recalled by Stryker Instruments...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Zipper Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Zipper Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versatex Monofilament Mesh 50 x 50cm Recalled by Sofradim Production Due to...
The Issue: There have been patient reports of abdominal hernia recurrence following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.