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. 2,702 recalls have been distributed to Nevada in the last 12 months.
Showing 4721–4740 of 28,334 recalls
Recalled Item: SW Bari Lift & Transfer Recalled by Raye's Inc. Due to Retrospective...
The Issue: Retrospective engineering analysis against current ISO standards for hoists...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: impression coping Recalled by Thommen Medical AG Due to The depth of the...
The Issue: The depth of the internal canal was not manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opal Recalled by Synthes (USA) Products LLC Due to Products not sterilized,...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDSORB IPS Battery Pack Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX Recalled by Synthes...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFNA Femoral Nail 9mm Recalled by Synthes (USA) Products LLC Due to Products...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5MM Drill Bit/QC/85MM Sterile-surgical Recalled by Synthes (USA) Products...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VA-LCP Clavicle Plate 2.7 Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5MM DRILL BIT/QC/GOLD/110MM STERILE-surgical Recalled by Synthes (USA)...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RIA Tube Assembly Recalled by Synthes (USA) Products LLC Due to Products not...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFNA Femoral Nail 11mm Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Adapter 4 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Catheter Ext. 18 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Catheter Ext. 6 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Safe Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health Waterproof Wound Tracking Dressing Recalled by MEDLINE...
The Issue: Product failed sterility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3.1...
The Issue: Potential interference with the anti-fall system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.