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. 2,722 recalls have been distributed to Nevada in the last 12 months.
Showing 2021–2040 of 50,223 recalls
Recalled Item: D2TCD Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C5-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L15-7IO TRANSDUCER Transducer Probe Recalled by Philips Ultrasound, Inc Due...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X7-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C9-5ec Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orascoptic Superior Visualization Custom loupes configured with Phantom...
The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L17-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C10-3v Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orascoptic Superior Visualization Phantom Essential kit ( Nose pad Recalled...
The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S8-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S12-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S7-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3-1 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SunBiotics Activated Almonds Infused with Probiotics Recalled by WINDY CITY...
The Issue: Salmonella Contamination. Firm detected salmonella on one batch of our...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg Recalled by Lupin...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE HealthCare OEC 9800. Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HealthCare OEC 9900 Elite C-arm Systems. Recalled by GE Medical Systems,...
The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sparrow Ascent Patient Controller Recalled by Spark Biomedical Inc Due to...
The Issue: Due to manufacturing issue, neurostimulator device may experience "cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SmartPump Tourniquet Recalled by Stryker Corporation Due to...
The Issue: Tourniquet cuff flange may become detached from the bladder. If leak occurs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT) Recalled by North American Rescue...
The Issue: Device used for unilateral or bilateral occlusion of blood flow to the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.