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 18581–18600 of 27,884 recalls
Recalled Item: Biograph mCT S(64)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT S(64)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the AxIEM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline E-Z Lubricating Jelly Recalled by MEDLINE IND Due to Product was not...
The Issue: Product was not sterilized. Product was shipped to distribution centers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope Recalled...
The Issue: Olympus is recalling the URF-P6/P6R endoscopes due to a similar device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Great Basin Staph lD/R Blood Culture Panel The Great Basin Recalled by Great...
The Issue: The Great Basin Staph ID/R Panel is being recalled because the S. aureus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The...
The Issue: Olympus has received complaints regarding the breakage of the endoscope's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rigid Laryngostroboscopes The Rigid Laryngostroboscopes Recalled by Pentax...
The Issue: Pentax is initiating a Field Correction to revise the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Recalled...
The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged...
The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System Recalled...
The Issue: Merge received reports of Merge Eye Station being unable to capture images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens initiated a corrective action to address two possible, mutually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products UPRO Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: There is a potential for variable negatively and positively biased urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N...
The Issue: Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/Q.zen Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens initiated a corrective action to address two possible, mutually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...
The Issue: Damaged packaging, lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...
The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.