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 19221–19240 of 27,884 recalls
Recalled Item: Integra Drainage Accessory Kits Recalled by Integra LifeSciences Corp. Due...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSA Dissectron Fingertip Laparoscopic Cannula Recalled by Integra...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera Biopsy Device Recalled by Hologic, Inc Due to Incorrect label on the...
The Issue: Incorrect label on the Sertera Biopsy Kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EKOS cart has the catalog number 700-60101. The EKOS Recalled by EKOS...
The Issue: Casters on the EKOS carts may be missing washers which can cause premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 Recalled by Panoramic Rental Corp. Due to...
The Issue: Panoramic Corporation is performing a voluntary Medical Device Correction on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HexaPOD evo RT System Product Usage: The intended use of Recalled by Elekta,...
The Issue: Potentially unrecognized incorrect position of the treatment couch in 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sagittal Blade 18.0X0.97X90MM Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling the Sagittal Blade...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Colonoscope is intended to be used with a Recalled by Pentax of...
The Issue: Pentax is initiating the product correction of several model numbers of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BruxZir Shaded Recalled by Prismatik Dentalcraft, Inc Due to Prismatik...
The Issue: Prismatik Dentalcraft is recalling BruxZir Shaded because the new design was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Gastroscope is intended to be used with a Recalled by Pentax of...
The Issue: PENTAX Medical is initiating this field action to provide customers that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific QMS Everolimus Assay Recalled by Microgenics Corporation...
The Issue: A reagent stability issue (still under investigation) causes less separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Fluid Management Set Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for Fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCR Compano Basic Reader using 100-127V as mains voltage. Model numbers:...
The Issue: A defect component of the Compano reader power supply can cause the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS versions 8.4.7 Recalled by Novarad Corporation Due to Novarad...
The Issue: Novarad Corporation announces a voluntary field action for the NovaPACS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a...
The Issue: Post Market Surveillance cases reported to Maquet showing instances in which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics, Inc. notified customers of erroneous results of VMA tests...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.