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. 1,077 recalls have been distributed to Nevada in the last 12 months.
Showing 11601–11620 of 28,334 recalls
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard BodySet Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset with Filter Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMExpress Microbore Sets Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset with Male Luer Connectors Recalled by CME America, LLC...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard BodySet with Needleless Connectors Recalled by CME America, LLC Due...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard set with Female Luer Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset with Filter and Manual Priming Valve Recalled by CME...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Recalled by...
The Issue: Convenience kit mislabeled with the incorrect catheter effective length on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay Luminex Recalled by Luminex Corporation Due...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay: Luminex Recalled by Luminex Corporation...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The Recalled by...
The Issue: During internal testing execution of the next generation of Integrated Power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuvasive NVM5 EMG Module Recalled by NuVasive Inc Due to The NVM5 EMG Module...
The Issue: The NVM5 EMG Module kit intended for intraoperative neurophysiologic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista one-piece hydrophobic acrylic toric intraocular lens Recalled by...
The Issue: The toric axis marks were misaligned (from the expected position in relation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.