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. 1,045 recalls have been distributed to Nevada in the last 12 months.
Showing 17181–17200 of 50,223 recalls
Recalled Item: TopCare Health Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOXOrubicin Hydrochloride Injection Recalled by Fresenius Kabi USA, LLC Due...
The Issue: Cross Contamination with Other Products: trace amounts of octreotide found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE...
The Issue: The firm is recalling their products due the unapproved use of a food...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...
The Issue: Zimmer Biomet is conducting a medical device correction to update the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...
The Issue: A software error was detected within software version 1.3.4 for the Tempus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Set Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream 35 Portable Respiratory Monitor Recalled by Covidien Llc Due to...
The Issue: The firm has released software update V01.05.02.16 (also known as V1.5.2) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Mg R1 - Product Usage: For the quantitative in Recalled by Randox...
The Issue: Failing to meet the linearity performance claims quoted on the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Rx Series Mg - Product Usage: For the quantitative Recalled by Randox...
The Issue: Failing to meet the linearity performance claims quoted on the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity ACL Tibial Elbow Guide-indicated for use in open and Recalled by...
The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity ACL Tibial Tip Guide- indicated for use in open Recalled by ConMed...
The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intellis Spinal Cord Stimulator Recalled by Medtronic...
The Issue: A710 Intellis Clinician Application has a software issue that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimulan Kit 10cc Recalled by Biocomposites, Ltd. Due to Mislabeling
The Issue: The product is mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.