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 1221–1240 of 28,334 recalls
Recalled Item: Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight Recalled by...
The Issue: Due to a weld breakage between the pin and inserter holder of the Inserter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to If the...
The Issue: If the radiosurgery system triggers a proximity error message during a long...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / Recalled by...
The Issue: Due to a manufacturing issue involving the silicone quad ring where the ring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Recalled by Olympus Corporation of the Americas Due to...
The Issue: Potential for the ESG-410 Electrosurgical Generator to display an error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Recalled by Olympus Corporation of the Americas Due to...
The Issue: Potential for the ESG-410 Electrosurgical Generator to display an error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...
The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Recalled by...
The Issue: The defect in the thread area will not allow the device to fully engage with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Recalled by...
The Issue: The defect in the thread area will not allow the device to fully engage with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOTAK RELIANCE G/SG with 4-SITE Connector Recalled by Boston Scientific...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELIANCE 4-FRONT Recalled by Boston Scientific Corporation Due to Affected...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOTAK RELIANCE G/SG Recalled by Boston Scientific Corporation Due to...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.