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. 2,702 recalls have been distributed to Nevada in the last 12 months.
Showing 4661–4680 of 50,223 recalls
Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to Due...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to Recalled by B Braun...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to Due to...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine HCl Injection Recalled by Fagron Compounding Services Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Varithena (polidocanol injectable foam) Administration Pack Recalled by...
The Issue: Defective Delivery System: incorrect silicone oil-free NormJect 10 mL Luer...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOW Real Foods Whole & Unsalted Raw Brazil Nuts 12oz. bag Recalled by Now...
The Issue: High mold, yeast, and total viable count
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TxHA PEEK IBF/TxTiHA IBF System i. TxHA The Recalled by Innovasis, Inc Due...
The Issue: Due to interfacing issues between the implant trial and inserter of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Premium SuperPulsed Laser - Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Pro SuperPulsed Laser Systems-Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Sheath Introducer 7.5F Recalled by Merit Medical Systems, Inc. Due...
The Issue: 7F sheath introducers labeled as 7.5F
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Procedure Kit Recalled by Merit Medical Systems, Inc. Due to 7F...
The Issue: 7F sheath introducers labeled as 7.5F
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (narrow indication)-Intended for...
The Issue: Product packaging process may result in an improper or incomplete seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation...
The Issue: Product packaging process may result in an improper or incomplete seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Seer Home System is an ambulatory electroencephalograph (EEG) system...
The Issue: During CAPA investigations of sight production inconsistencies, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective Container: patients are unable to get the solution out of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ibuprofen 800mg Recalled by Direct Rx Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: Product failed impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STERILIZABLE INTERNAL DEFIBRILLATION PADDLES STERILIZABLE INTERNAL...
The Issue: Due to customer complaints and out of box failures, the firm is conducting a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.