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. 2,551 recalls have been distributed to Nevada in the last 12 months.
Showing 19461–19480 of 28,334 recalls
Recalled Item: Transpac¿ IV Monitoring Kit w/Safeset 72" Pressure Tubing Recalled by ICU...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONITORING KIT WITH 03ML FLUSH DEVICE FOR LEHIGH VALLEY HOSPITAL CENTER...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSPAC¿ IV MONITORING KIT DISPOSABLE TRANSDUCER Recalled by ICU Medical,...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double LINE SAFESET" KIT WITH 03ML FLUSH DEVICE FOR E.U.S.H.C. Recalled by...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUAD TRANSDUCER KIT WITH 03ML FLUSH DEVICE FOR LUBBOCK HEART HOSP. Recalled...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-MR1 Ventilator: Catalog# 161010 The Hamilton MR1 Ventilator is...
The Issue: Oxygen tubing and the oxygen connector of the Hamilton-MR1 could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioSentry Tract Sealant System Recalled by Surgical Specialties Mexico S DE...
The Issue: Surgical Specialties Mexico is recalling the BioSentry Track Sealant System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V. Mueller Neuro/Spine Recalled by Cardinal Health 200, LLC Due to Potential...
The Issue: Potential risk associated with corrosion demonstrated on the distraction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A Recalled by Merit...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluid Management Set. Catalog Number K08-MP5159A Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waste Management Kit. Catalog Number K10-04381AP Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold Kit. Catalog Number K09-11867AP Recalled by Merit Medical Systems,...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Brivo 715 Prime Recalled by GE OEC Medical Systems, Inc Due to GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC Brivo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Kit (MeriTrans"). Catalog Number K11-00232G Recalled by...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation O-arm O2 Surgical Imaging System Product Catalog...
The Issue: O-arm O2 Surgical Imaging System Spatial calibration may be erroneous in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBRA Fusion 50 Ablation System Recalled by AtriCure, Inc. Due to Due to...
The Issue: Due to product design and process control, part of the device can separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product...
The Issue: There is a potential for a component failure of the device which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD79b PE (ASR) Recalled by Becton, Dickinson and Company, BD Biosciences Due...
The Issue: CD79b (SN8) PE is contaminated with a FITC conjugate of unknown antigenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product...
The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Pressure Tourniquet Cuff (PTC) Tourniquet cuffs are single- or...
The Issue: Issue with the process for detection of leaking Pressure Tourniquet Cuffs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.