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. 2,696 recalls have been distributed to Nevada in the last 12 months.
Showing 6121–6140 of 50,223 recalls
Recalled Item: Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage Recalled by Andover...
The Issue: A packaging seal gap could impact the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airvo 2 Humidifier Recalled by Fisher & Paykel Healthcare, Ltd. Due to...
The Issue: Humidifier devices, used to deliver high flow respiratory therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: Charles Boggini Company Cola Flavoring Base Recalled by Charles Boggini...
The Issue: Products contain undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Charles Boggini Pink Lemonde Recalled by Charles Boggini Company Llc Due to...
The Issue: Products contain undeclared FD&C Red No. 40
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Charles Boggini Company Yellow Lemonade and Yellow Lemonade X Recalled by...
The Issue: Products contain undeclared FD&C Yellow No. 5
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Eyesaline Recalled by HONEYWELL INC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: Atovaquone Oral Suspension USP Recalled by AvKARE Due to Microbial...
The Issue: Microbial contamination of a non-sterile product: potential Bacillus cereus...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isotretinoin Capsules Recalled by Teva Pharmaceuticals USA, Inc Due to...
The Issue: Superpotent Drug: The 3-month stability result for assay was found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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.