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. 1,786 recalls have been distributed to Nevada in the last 12 months.
Showing 39981–40000 of 50,223 recalls
Recalled Item: 5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CS 8100 Recalled by Carestream Health, Inc. Due to Units device head...
The Issue: Units device head descended unexpectedly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 8100 3D Recalled by Carestream Health, Inc. Due to Units device head...
The Issue: Units device head descended unexpectedly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This correction applies to all GE Healthcare MRI systems with Recalled by GE...
The Issue: At certain sites, the MRU may not be connected to the magnet. In emergency...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cold Therapy Pad - cold water circulating pad Recalled by Cincinnati...
The Issue: Seals in the water path of the CT-99 cold therapy pad may separate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings Recalled by...
The Issue: Stryker is recalling System 6 Aseptic Housing, due to a failed Continuous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benzonatate Capsules Recalled by American Health Packaging Due to Failed...
The Issue: Failed Tablet/Capsule Specifications; recall initiated by manufacturer due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GROUND CUMIN SEED Recalled by Morris J. Golombeck, Inc. Due to Undeclared Peanut
The Issue: Cumin may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Walnut Pieces packaged in the following sizes and brand names: Recalled by...
The Issue: Product may be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Ebb Complete Tamponade System Recalled by Clinical Innovations, LLC Due...
The Issue: Clinical Innovations, LLC is voluntarily recalling the Ebb Complete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW Epidural Needle Component (product number AN-05501). Epidural needles...
The Issue: The product labeling does not specify the 5 year shelf life of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Whole Foods Market Small Cookie Platter 18oz. Code: 24386800000 Recalled by...
The Issue: The firm is recalling Whole Foods Market Cookie Platter Small. Medium, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EPWorks software used in the Xltek Protektor Stimulator Product Usage:...
The Issue: Software error occurs when using remote monitoring; if the remote user tries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPWorks software used in the Protektor 32 Product Usage: Uses Recalled by...
The Issue: Software error occurs when using remote monitoring; if the remote user tries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The...
The Issue: Foreign material found within the kits. The foreign material, white or black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hummus Recalled by Zilks Foods Due to Undeclared Peanuts
The Issue: Potential undeclared peanuts in cumin ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hummus Recalled by Zilks Foods Due to Undeclared Peanuts
The Issue: Potential undeclared peanuts in cumin ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hummus Recalled by Zilks Foods Due to Undeclared Peanuts
The Issue: Potential undeclared peanuts in cumin ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hummus Recalled by Zilks Foods Due to Undeclared Peanuts
The Issue: Potential undeclared peanuts in cumin ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hummus Recalled by Zilks Foods Due to Undeclared Peanuts
The Issue: Potential undeclared peanuts in cumin ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.