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. 1,045 recalls have been distributed to Nevada in the last 12 months.
Showing 17381–17400 of 50,223 recalls
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) Ventilator Series - Product Usage: for Recalled...
The Issue: In-house lab observations and customer reports of overheating and/or thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elderberry Whole Organic Recalled by Starwest Botanicals, Inc Due to...
The Issue: Direct customer tested product upon receipt and had a positive result for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elderberry Whole Organic Recalled by Starwest Botanicals, Inc Due to...
The Issue: Direct customer tested product upon receipt and had a positive result for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in Recalled by Ra...
The Issue: Due to footswitch not meeting required specification for protection from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous...
The Issue: 5F Micro-Introducer Kits may not contain the correct device, packaged with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...
The Issue: Luminex has determined that three (3) separate test fixtures used by field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...
The Issue: Luminex has determined that three (3) separate test fixtures used by field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard - Product Usage: Obstetric Gynecologic specialized manual instrument....
The Issue: Labeling error, incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Recalled by...
The Issue: Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Happy Kid Gluten Free Fruit & Oat Bar Organic Blueberry Recalled by Nurture...
The Issue: Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Happy Tot Superfoods Gluten Free Oat Bar Organic Bananas Recalled by Nurture...
The Issue: Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Spice Hunter California Garlic 2.7 oz. Jar Recalled by Sauer Brands Inc...
The Issue: Potential Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.