Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,582 recalls have been distributed to Delaware in the last 12 months.
Showing 15761–15780 of 27,373 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: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...
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: PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes may...
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: 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: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...
The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...
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: Neonatal PICC 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: Maximum Barrier Insertion Tray Recalled by Vygon U.S.A. Due to Potential...
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: PICC Kit Recalled by Vygon U.S.A. Due to Potential friction holes may affect...
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: 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) 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: 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: 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: 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: 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: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...
The Issue: Wire sets of certain devices were assembled with adhesive on the contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATHETER REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.