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 3121–3140 of 28,334 recalls
Recalled Item: Aligned Medical Tonsil Tray that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Septo Pack that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical T and A Pack that contains Recalled by Windstone Medical...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Tonsil Pack that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Tonsil ENT Pack that contains the Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatine Kinase (CK) used on cobas c 311/501/502 and COBAS Recalled by Roche...
The Issue: Creatine Kinase (CK) Assay Abnormal calibrations on the cobas¿ c 311/501/502...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: STREAMLINE LONG-Tubing to be used to transfer blood between a Recalled by B...
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 PCA Module Model 8120 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: Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring...
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: Atellica CH Microalbumin_2 (¿ALB_2)-For in vitro diagnostic use in the...
The Issue: Atellica CH Microalbumin_2 (¿ALB_2) and the ADVIA Chemistry Microalbumin_2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Microalbumin_2 (¿ALB_2) -For in vitro diagnostic use in...
The Issue: Atellica CH Microalbumin_2 (¿ALB_2) and the ADVIA Chemistry Microalbumin_2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE BLOODLINE LONG VERSION Recalled by B Braun Medical Inc Due to...
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 Syringe Module Model 8110 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: STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to Recalled by B...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.