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. 2,726 recalls have been distributed to Nevada in the last 12 months.
Showing 41–60 of 50,223 recalls
Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INFUSION Recalled by B Braun...
The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Recalled by B...
The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 700 AU Recalled by Beckman Coulter Mishima K.K. Due to A delay in...
The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit:...
The Issue: The instructions for use (IFUs) on specified Cardinal Health Chest Drainage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Tuna Salad product container is mislabeled with a Chicken Salad lid...
The Issue: Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HealthCast "Vital Sync" Remote Patient Monitoring System which consists of:...
The Issue: Due to complaints and investigations stating that alarms from the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHEMISTRY ANALYZER AU5800 Recalled by Beckman Coulter Mishima K.K. Due to A...
The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units...
The Issue: Potential for rubber fragment detachment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units...
The Issue: Potential for rubber fragment detachment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE Recalled by Medline...
The Issue: Fabric may experience premature delamination when using included laundering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN Recalled by Medline...
The Issue: Fabric may experience premature delamination when using included laundering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Why Not Natural Moringa Capsules 120 capsule bottle marked with Recalled by...
The Issue: Potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Impella RP with SmartAssist. Product Code: 0046-0035. Recalled by Abiomed,...
The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist. Product Code: 1000323. Recalled by...
The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITY II Laser System Recalled by Lutronic Corporation Due to Reports of...
The Issue: Reports of devices sparking/popping and potentially burning patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029....
The Issue: During the bulk packaging process, some Luer Slip syringes were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.