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. 2,722 recalls have been distributed to Nevada in the last 12 months.
Showing 1861–1880 of 50,223 recalls
Recalled Item: DermaKleen Recalled by DermaRite Industries, LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KleenFoam Recalled by DermaRite Industries, LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SureStep Foley Tray System Bardex I.C. Complete Care Infection Control...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray Recalled by...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant...
The Issue: Measles IgM Test Kit lacks premarket approval or clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Pack Recalled by O&M HALYARD INC Due to Surgical drape packs may...
The Issue: Surgical drape packs may have open seals, which may compromise the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPC Powerease System UDI-DI: 00613994448705 00643169406834. The IPC Recalled...
The Issue: Due to out of the box wobble of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle 3 with TumorLOC Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: Due to software issue, Radiation Therapy Planning system may provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Intended use:...
The Issue: Product may have small flakes of stainless steel in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended use: Recalled by...
The Issue: Product may have small flakes of stainless steel in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Intended use:...
The Issue: Product may have small flakes of stainless steel in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sushi Wasabi Recalled by MING HONG INTERNATIONAL INC. Due to Individual...
The Issue: Individual consumer size Wasabi mini pack label does not declare allergen...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TOPS Inserter Recalled by PREMIA SPINE LTD Due to Potential for missing pins...
The Issue: Potential for missing pins at tip of inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chromophare Surgical Light System Recalled by Stryker Communications Due to...
The Issue: Surgical lights have stress lines forming on the powder coating, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosthesis Head B Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Inconsistent size terminology and color coding used on labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Trial Head Brown Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: Inconsistent size terminology and color coding used on labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pure Monk Fruit Sweetener Recalled by NuNaturals Inc Due to Product is...
The Issue: Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Pure Stevia Recalled by NuNaturals Inc Due to Product is Monk Fruit...
The Issue: Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
Recommended Action: Do not consume. Return to store for a refund or discard.