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. 2,493 recalls have been distributed to West Virginia in the last 12 months.
Showing 11861–11880 of 27,884 recalls
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemashield Gold Knitted Microvel Double Velour Vascular...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Accelerator a3600 Recalled by Inpeco S.A. Due to When analyzer sample...
The Issue: When analyzer sample carousel lid remains open or manual process is too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model:...
The Issue: If the shaft breaks due to material fatigue, the trauma arm can fall down...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemashield Gold Knitted Microvel Double Velour Vascular Graft...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation System using the Aliquoter Module (Inpeco P/N FLX-212)...
The Issue: In certain firmware versions, in case a Clot Detection error (error code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oryx Cervical Screw Caddy Recalled by Innovasis, Inc Due to Cervical screw...
The Issue: Cervical screw caddies have incorrect text markings for the 4.5mm Fixed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SKAFFOLD FLOW (MX) 5CC. Product Number: SKMX-FL05 Recalled by Skeletal...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION EX Recalled by Skeletal Kinetics, Llc Due to Bone void filler...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH OSSILIX MP FIL Recalled by Skeletal Kinetics, Llc Due to Bone void...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRANIOSCULPT FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void filler...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRANIOSCULPT FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void filler...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATIONEX 5CC Recalled by Skeletal Kinetics, Llc Due to Bone void filler...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEOVATION RMX 10CC. Product Number: 390-6002 Recalled by Skeletal...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SKAFFOLD CMF IMPRESS (MP) Recalled by Skeletal Kinetics, Llc Due to Bone...
The Issue: Bone void filler kits may not maintain its setting characteristics for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.