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. 1,715 recalls have been distributed to Nevada in the last 12 months.
Showing 44841–44860 of 50,223 recalls
Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...
The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...
The Issue: Integra LifeSciences has identified through an internal evaluation that in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Luer Lock Cap The device is intended for use Recalled by Baxter...
The Issue: The firm is recalling lots 10043 and 10044 due to loose particulate matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...
The Issue: STERIS has identified that the population of the G. stearothermophilus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...
The Issue: Expired active ingredient was used in the manufacture of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...
The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...
The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube Recalled by Becton...
The Issue: An in-vitro diagnostic reagent may be labeled with an incorrect barcode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 14951-48 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 19734-28 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 19683-28 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi Complete (Full Strength Mini and Multi Softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi For Him (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.