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. 2,595 recalls have been distributed to Nevada in the last 12 months.
Showing 17281–17300 of 28,334 recalls
Recalled Item: RayStation Product Usage: is a software system designed for treatment...
The Issue: For the proton QA preparation module in RayStation 6 (including SP1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TD60 Transmitter battery charger used with the BeneVision Central Station...
The Issue: A damaged circuit board in the battery charger can cause the battery to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC-1000 Recalled by Panoramic Rental Corp. Due to The lift motor used to...
The Issue: The lift motor used to raise and lower the overhead chassis will wear if not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A3/A5 Anesthesia Delivery System Recalled by Mindray DS USA, Inc....
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba...
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Euphora Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ReNew Reusable Grasper and Dissector Tips are to be Recalled by...
The Issue: The heat-shrink insulation tube may split during autoclave...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERMI250 Radiofrequency System. Intended to provide heating for the purpose...
The Issue: In some systems, the unit continues to emit RF energy after the PAUSE button...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP - Model 728311 Brilliance iCT - Model Recalled by Philips...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT - Model 728306 Computed Tomography X-ray systems Recalled by...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA...
The Issue: Instruments may, under certain specific circumstances listed below, fail to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondamed Biofeedback Device Recalled by Ondamed Inc Due to The firm was...
The Issue: The firm was marketing the Ondamed System in the US without marketing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.