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. 1,712 recalls have been distributed to Nevada in the last 12 months.
Showing 47181–47200 of 50,223 recalls
Recalled Item: Allen Traction Boot Recalled by Allen Medical Systems, Inc. Due to Some...
The Issue: Some units may have been assembled incorrectly which could result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See's Candies Recalled by See's Candies Inc. Due to One code of 1.7 oz...
The Issue: One code of 1.7 oz Divinity Easter Eggs with Walnuts may actually contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sirtex SIR-yttrium 90 microspheres (Radionuclide) Recalled by Sirtex Medical...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Venous blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is Recalled...
The Issue: Medtronic has found through device testing that if the optional footswitch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Risk that air...
The Issue: Risk that air may be introduced into the device which may lead to an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers :...
The Issue: Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Labeling Wrong Barcode; It may display wrong product code 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIBRICOR (fenofibric acid) Tablets Recalled by Mutual Pharmaceutical...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge Recalled by...
The Issue: Straight needle labeled as a curved needle
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Acetate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.