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. 2,696 recalls have been distributed to Nevada in the last 12 months.
Showing 5441–5460 of 28,334 recalls
Recalled Item: FIRST RESPONSE 2 CT Recalled by Family Dollar Stores, Llc. Due to Products...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARC TEETH WHITENING PEN 0.06 FL OZ Recalled by Family Dollar Stores, Llc....
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORAL B MOUTH SORE RINSE 237ML Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT Recalled by Family Dollar Stores,...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Patient Electronic System (PES) Recalled by St. Jude Medical Due...
The Issue: Potential for damaged and frayed power connector plug with repeated bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GOODSENSE DENTURE CLEANSER GRN TAB 40CT Recalled by Family Dollar Stores,...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIXODENT ORG CREAM 2.4OZ Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIQUICK PREGNANCY TEST 1CT Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HILLROM PROGRESSA+ BED Recalled by Baxter Healthcare Corporation Due to...
The Issue: Progressa+ beds have the potential for static buildup from the casters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...
The Issue: Elevated results were detected with Li-heparin plasma samples when compared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edge Biologicals STERILE WATER Recalled by Edge Biologicals Inc Due to Due...
The Issue: Due to product outer packaging incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...
The Issue: Unexpected failure of electrical components within the CPI generator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...
The Issue: Deterioration in the stability of the Test Strips results in diminished...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...
The Issue: Sterilization failures when devices are sterilized per the Reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...
The Issue: There is a potential for unexpected failure of the electrical components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt Dome Electrode Recalled by Coapt LLC Due to Patient may experience...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVO +VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.