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. 2,684 recalls have been distributed to Nevada in the last 12 months.
Showing 8701–8720 of 50,223 recalls
Recalled Item: Exactech Shoulder GPS Impactor Handle Recalled by Exactech, Inc. Due to The...
The Issue: The ball and spring housed within the locking mechanism of the handle can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Cytosponge Cell Collection Device Recalled by Covidien, LLC Due to...
The Issue: Cell Collection Device may be at increased risk of the sponge detaching from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxA Automation System Recalled by Beckman Coulter Biomedical...
The Issue: A software defect in the DxA Automation System may cause tests to be run on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxA Automation System Recalled by Beckman Coulter Biomedical...
The Issue: A software defect in the DxA Automation System may cause tests to be run on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg Recalled by The Harvard Drug Group...
The Issue: Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Shots were...
The Issue: Shots were terminated by the mAs integrator; however, the 4 ms exposure time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trexo Device Recalled by Trexo Robotics Holdings Inc. Due to Electrical...
The Issue: Electrical issues that could potentially render the device non-functional,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UFSK Treatment chair 500 XLE- Treatment chair for positioning and Recalled...
The Issue: Service life of the electrical seat part drive of the treatment chair may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Osteomed, LLC Due to Screws for osteotomies have contain an...
The Issue: Screws for osteotomies have contain an undersize screwhead which has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Osteomed, LLC Due to Screws for osteotomies have contain an...
The Issue: Screws for osteotomies have contain an undersize screwhead which has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Specific...
The Issue: Specific diluent lot numbers showed that conductivity, osmolality, and pH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium (Agar) (150mm) Recalled by Remel, Inc Due to...
The Issue: The test medium may not perform as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.