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. 2,510 recalls have been distributed to Nevada in the last 12 months.
Showing 24701–24720 of 28,334 recalls
Recalled Item: Optiflux F200NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F180NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...
The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200A High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu AlB & RSV Direct Assay Kits Recalled by Focus Diagnostics Inc...
The Issue: Focus Diagnostics initiated the recall of the certain Simplexa Flu AlB & RSV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F18Nre Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F180NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Recalled by Siemens Medical Solutions Diagnostics Due to There...
The Issue: There is a potential for incorrect results to be reported from processing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mega-Gen His Personal Lubricant Recalled by Altasource LLC dba Meta Labs LLC...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citation TMZF HA 132 degrees Neck Angle Recalled by Stryker Howmedica...
The Issue: Stryker received a report from the field indicating that a citation TMZF HA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...
The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...
The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot Ice Recalled by Altasource LLC dba Meta Labs LLC Due to Firm is not...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Treatment packs used on the VisuMax Laser Keratome. Size M Recalled by Carl...
The Issue: Carl Zeiss Treatment pack, lot number M 130010, size M, may actually contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nice-En-Smooth Berry Burst Recalled by Altasource LLC dba Meta Labs LLC Due...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amo-O Herbal Stimulator Recalled by Altasource LLC dba Meta Labs LLC Due to...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.