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. 2,706 recalls have been distributed to Nevada in the last 12 months.
Showing 4261–4280 of 28,334 recalls
Recalled Item: OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124...
The Issue: Device may experience an interruption or loss of therapy in case of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER Application Instrument Recalled by Karl Storz Endoscopy Due to Laser...
The Issue: Laser surgical instruments have no specific evidence of a validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A...
The Issue: Due to unsupported 10 year expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version:...
The Issue: Due to unsupported 10 year expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Oncology Essentials Package of the Spectral CT imaging system. Recalled...
The Issue: Potential for third party oncology marking laser to be off the gantry cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1 Recalled by Stryker Leibinger GmbH & Co. KG Due to Mislabeling
The Issue: Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HORIBA custom configured fluorescence instrument Recalled by Horiba...
The Issue: HORIBA custom configured fluorescence instrument has a laser safety defect....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 13.0.0.1547 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 8.1.0.47 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9.0.0.113 and 9.0.1.142. Radiation Therapy Treatment Planning...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 11.0.0.951 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 8.0.0.61 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 15.0.0.430. Radiation Therapy Treatment Planning System. Recalled...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 7.0.0.19. Radiation Therapy Treatment Planning System. Recalled...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 10.0.0.1154 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 10.1.0.613 and 10.1.1.54. Radiation Therapy Treatment Planning...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 12.0.0.932 Recalled by RAYSEARCH LABORATORIES AB Due to Potential...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 14.0.0.3338. Radiation Therapy Treatment Planning System....
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 9.1.0.933 and 9.2.0.483. Radiation Therapy Treatment Planning...
The Issue: Potential for reported SSD to be too high.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-Flex Femoral Component Recalled by Zimmer, Inc. Due to Out of...
The Issue: Out of specification violation of devices that results in a gap existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.