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. 2,044 recalls have been distributed to Nevada in the last 12 months.
Showing 5621–5640 of 28,334 recalls
Recalled Item: Vasc. Open CVOR SJH Recalled by American Contract Systems, Inc. Due to...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS PCSU SJH Recalled by American Contract Systems, Inc. Due to During an...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Heart SJH Recalled by American Contract Systems, Inc. Due to...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Pack Recalled by American Contract Systems, Inc. Due to During an...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cath Cardiac Pack Recalled by American Contract Systems, Inc. Due to During...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sub Q Recorder Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Urology Wolson Pack Recalled by American Contract Systems, Inc....
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: The Guardian System Product Name: The Guardian Model/Catalog...
The Issue: Device reaching End of Service prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroPICC 5Fr Dual Lumen Maximal Barrier Kit Recalled by Access Vascular,...
The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT...
The Issue: The firm conducting a recall due to a complaint received indicating that a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zephyr Endobronchial Valve (EBV) 5.5-LP Recalled by Pulmonx, Corp. Due to...
The Issue: Endobronchial implant devices may have been labeled with a shortened...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vitals Monitor Recalled by Philips North America Llc Due to A...
The Issue: A software issue prevents the monitor from alarming when the high/low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroPICC 5Fr Dual Lumen Recalled by Access Vascular, Inc Due to Specific...
The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vital Signs Monitor Recalled by Philips North America Llc Due...
The Issue: A software issue prevents the monitor from alarming when the high/low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API3200MD Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CellQuicken Analyzer (Smart-Watch and Software) Recalled by RoyalVibe Health...
The Issue: Ultrasound devices were not authorized, cleared, or approved by FDA, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citrine QTRAP Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...
The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.