Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,437 recalls have been distributed to West Virginia in the last 12 months.
Showing 19121–19140 of 27,884 recalls
Recalled Item: Expression MR IBP DPT Kit Recalled by ICU Medical, Inc. Due to 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: Cath Lab Kit w/03 ml Squeeze Flush Recalled by ICU Medical, Inc. Due to 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: Transpac¿ IV Monitoring Kit Recalled by ICU Medical, Inc. Due to 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: KIT W/30ML FLUSH DEVICE FOR ALL CHILDRENS Hospital 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: TRANSDUCER KIT W/30ML FLUSH DEVICE FOR CHILDRENS HOSP. OF WISC. 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: OPEN HEART MONITORING KIT WITH 03ML FLUSH DEVICE FOR ORLANDO REG. MED. CTR....
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: SAFESET" KIT W/03ML FLUSH DEVICE FOR HOLMES REG. M.C. 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: Roche COBAS INTEGRA c111 Analyzer Recalled by Roche Diagnostics Operations,...
The Issue: cobas c 111 analyzers (catalog numbers 04777433001 and 04528778001) with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The surgical table is a stand alone unit. Three (3) Recalled by Schaerer...
The Issue: The floor locking cylinders contained in the base of the Schaerer 7300 model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heater Cooler Unit Usage: The Heater-Cooler Unit (HCU 30) supplies Recalled...
The Issue: There is the potential for contaminated water to enter parts of the...
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: 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: VIA 27 Microcatheter Recalled by Sequent Medical Inc Due to Sequent Medical...
The Issue: Sequent Medical is recalling the VIA 27 Microcatheter because it may not...
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: 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: 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: 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: 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: 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: 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.