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. 1,729 recalls have been distributed to West Virginia in the last 12 months.
Showing 40661–40680 of 48,376 recalls
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Linear Accelerators of type ARTISTE Recalled by Siemens Medical...
The Issue: A safety risk exists with automatically sequenced treatment technique using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navitas Naturals Organic Sprouted Chia Powder Recalled by Navitas, LLC., dba...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: William & Sonoma Navitas Naturals brand Omega 3 Smoothie Mixer Recalled by...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Navitas Naturals Omega Blend Sprouted Smoothie Mix Recalled by Navitas,...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Large Pitted Kalamata Olives Recalled by Dot Foods Inc. Due to This...
The Issue: This voluntary recall has been initiated because Savor Brands Large Pitted...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Langston Dual Lumen Catheters Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner catheter of some Langston V2 Dual Lumen Catheters have separated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FirmArray Blood Culture Identification (BCID) Panel Recalled by BioFire...
The Issue: BioFire has identified an increased risk of false positive results when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Although the Natural Rubber Latex...
The Issue: Although the Natural Rubber Latex caution symbol is clearly displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Recalled by Elekta, Inc. Due to When using CMA, if the user hovers the...
The Issue: When using CMA, if the user hovers the mouse pointer exactly above the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or Recalled by...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Stem Standard & Extended Offset Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Reduced Neck Standard & Extended Offset Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Soft-arc Aortic Cannula 8.0mm curved tip Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.