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. 2,659 recalls have been distributed to Nevada in the last 12 months.
Showing 11481–11500 of 50,223 recalls
Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4712 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6566 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Banana Boat hair & scalp defense Recalled by Edgewell Personal Care Brands,...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations:OOS result was observed in 1-Methyl-4-Nitroso Piperazine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Extended Release Tablets Recalled by Amneal...
The Issue: Failed dissolution specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine for Injection Recalled by Amerisource Health Services LLC Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ORCA FOAM STANDARD CUBE 10x10x10 mm Recalled by GELITA MEDICAL GMBH Due to...
The Issue: In routine bioburden testing, higher than acceptable levels of Endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco Medical Network Adapter Recalled by BARCO NV Due to installation issues
The Issue: installation issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone Recalled...
The Issue: An incorrect sizing label was applied to the carton packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute...
The Issue: (1)Software version 2.74 upgrade and (2)hardware related cause that affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diasol Acid Concentrate 100 Recalled by Diasol, Inc Due to Due to labeling...
The Issue: Due to labeling issue. The box label is different that the gallon label in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...
The Issue: Potential for Vanta Clinician Programmer Application (CP App) A71200...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT STAT Troponin-I Reagent Kit Recalled by Abbott Laboratories Due to...
The Issue: One lot of reagent was manufactured with insufficient quantities of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...
The Issue: Potential communication issue in which the Vanta Clinician Programmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acidified Concentrate Distribution and Storage-The Isopure ACDS (Acidified...
The Issue: Acidified Concentrate Distribution System potential electrical safety hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5" Recalled by Stradis Medical,...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Scissors Iris Curved 4.5" Recalled by Stradis Medical,...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nobel Biocare N1 TiUltra TCC NP 3.5x13mm Recalled by Nobel Biocare Due to...
The Issue: Due to the presence of a burr which may cause an aspiration risk to patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5" Recalled by Stradis...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fentaNYL Citrate in 0.9% Sodium Chloride Recalled by SterRx, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.