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. 2,651 recalls have been distributed to Nevada in the last 12 months.
Showing 13341–13360 of 50,223 recalls
Recalled Item: Nature's Eats Balance Hearty Mix 16 oz. packaged Recalled by Texas Star Nut...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nature's Eats Nut for Life Balance Mix 12 oz. Recalled by Texas Star Nut and...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HCG 6 Recalled by Revive Rx LLC dba Revive Rx Pharmacy Due to Non-sterility;...
The Issue: Non-sterility; bacterial contamination identified as Paenibacillus lautus.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Woody's Smokehouse brand Yogurt Raisins Recalled by Lehi Valley Trading Co,...
The Issue: Bags and tubs of yogurt covered raisins contained undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CombiDiagnost R90 1.1 (709031) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 (709030) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUNTLEIGH Disposable intraoperative Probe Recalled by Huntleigh Healthcare...
The Issue: Faceplate may become detached from the probe body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4-11B Recalled by RaySearch America Inc Due to Incorrect source...
The Issue: Incorrect source to skin or surface distance (SSD) calculation may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Integrated Reaction Units (IRU) Recalled by Abbott Molecular, Inc....
The Issue: There is potential for the Reaction Vessels (RVs) detaching from the RV cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RISE UP RED EDITION Capsules Recalled by Positive Health Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avaphinal Maximum Male Enhancement Sexual Pills Recalled by Walmart Stores...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Oral Solution (Concentrate) Recalled by Lannett Company, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fresh Enoki Mushrooms 5.25oz/150 g/ 34 packages per case Recalled by Concord...
The Issue: California Department of Public Health sampled product and found it to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atellica CH Fructosamine (Fruc) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.