Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,608 recalls have been distributed to Nevada in the last 12 months.
Showing 16381–16400 of 28,334 recalls
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: 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: 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: 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 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: 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: GE Healthcare Centricity PACS-IW Recalled by GE Healthcare Due to A database...
The Issue: A database handling error could occur during the image acquisition process...
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: 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: 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: 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: 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: 12F Tesio CATHETER SET (CUFF 32CM FROM TIP) Recalled by Medical Components,...
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: 12F X 40CM TESIO CATHETER SET WITH "Y" ADAPTOR Recalled by Medical...
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: 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.