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. 2,450 recalls have been distributed to West Virginia in the last 12 months.
Showing 18321–18340 of 27,884 recalls
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx38cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xl por st 24.0x220mm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx48cm left Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis fluoroscopic x-ray system Recalled by Siemens Medical Solutions...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400 Recalled by Welch...
The Issue: A defective electrical component in the battery charging circuit in two lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.Zen fluoroscopic x-ray system Recalled by Siemens Medical...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego fluoroscopic x-ray system Recalled by Siemens Medical...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Brain 3.0 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Spine 1.0.2 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView SPECT model number 882480 BrightView and BrightView X are...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT model number 882482 BrightView and BrightView X are Recalled...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X 3/4 model number 882479 BrightView and BrightView X Recalled by...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...
The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X 3/8 model number 882478 BrightView and BrightView X Recalled by...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...
The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.