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 18881–18900 of 27,884 recalls
Recalled Item: BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating Large Craniotome Recalled by The Anspach Effort, Inc. Due to...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 16CM MIN INVASIVE ATTACH Recalled by The Anspach Effort, Inc. Due to...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Console Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AL-III-DISS Adapter Product Usage: Pneumatic system Recalled by The Anspach...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11CM ANGLE ATTACHMENT Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eMax2 Hybrid Hand Control Product Usage: Electric system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compact Speed Reducer Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11cm QD Angle Attachment Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STANDARD CRANIOTOME Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Console Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electronic Foot Control with Direction Switch Product Usage: Electric system...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12.6CM TAPERED ATTACHMENT Recalled by The Anspach Effort, Inc. Due to...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XMAX Motor Recalled by The Anspach Effort, Inc. Due to Supplied Directions...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14cm QD Angle Attachment Product Usage: Product attachment Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRI AIR CONTROL Product Usage: Pneumatic system Recalled by The Anspach...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMALL ATTACHMENT Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.8cm Controlled Depth Attachment Product Usage: Pneumatic system Recalled...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric Handpiece EM Hand Control Product Usage: Electric system Recalled...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14cm QD Angle Attachment Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.