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 621–640 of 50,223 recalls
Recalled Item: Cisatracurium Besylate Injection USP Recalled by SOMERSET THERAPEUTICS LLC...
The Issue: Subpotent product:out of specification assay results observed during long...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL) Recalled by...
The Issue: Correct Labeled Product Mispack-Size stated on carton label did not match...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter UniCel Dxl 600 Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has determined that, due to a potential communication issue,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter UniCel Dxl 800 Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has determined that, due to a potential communication issue,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive...
The Issue: Butyrate tube cracks during actuation, rendering product unusable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 Sensor UDI-DI code: 00357599818005 The Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
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 the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599844011 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599843014 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599819002 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...
The Issue: For certain customers, the Change Summary review option ceases to operate as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.