Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,553 recalls have been distributed to Alabama in the last 12 months.
Showing 16521–16540 of 28,641 recalls
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: 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: 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) 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: 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: 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: 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: 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 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 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.
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: 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 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 (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: 12F MODIFIED Tesio CATHETER SET Recalled by Medical Components, Inc dba...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.