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. 2,353 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,353 in last 12 months

Showing 3090130920 of 48,376 recalls

Medical DeviceOctober 11, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RF MultiGen¿ Recalled by Stryker Instruments Div. of Stryker Corporation Due...

The Issue: Stryker Instruments is voluntarily recalling the Care...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceOctober 11, 2016· Abbott Laboratories

Recalled Item: ARCHITECT Lactic Acid Part # 09D891T21 The Lactic Acid assay Recalled by...

The Issue: Abbott has identified negative interference from the drug N-Acetyl Cysteine...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: Radiation Therapy Treatment Planning System Product Usage: RayStation is a...

The Issue: An error may occur with the display of dose computed on images other than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodOctober 11, 2016· Chocolate Shoppe Ice Cream Co., Inc.

Recalled Item: Sticks & Stones Ice Cream Recalled by Chocolate Shoppe Ice Cream Co., Inc....

The Issue: The Chocolate Chip Cookie Dough pieces in the ice cream have the potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 11, 2016· Chocolate Shoppe Ice Cream Co., Inc.

Recalled Item: Yippee Skippee Ice Cream Recalled by Chocolate Shoppe Ice Cream Co., Inc....

The Issue: The Chocolate Chip Cookie Dough pieces in the ice cream have the potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 11, 2016· Chocolate Shoppe Ice Cream Co., Inc.

Recalled Item: Peanut Butter Cookie Dough Ice Cream Recalled by Chocolate Shoppe Ice Cream...

The Issue: The Chocolate Chip Cookie Dough pieces in the ice cream have the potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 11, 2016· Chocolate Shoppe Ice Cream Co., Inc.

Recalled Item: Heaps of Love Ice Cream Recalled by Chocolate Shoppe Ice Cream Co., Inc. Due...

The Issue: The Chocolate Chip Cookie Dough pieces in the ice cream have the potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 11, 2016· Chocolate Shoppe Ice Cream Co., Inc.

Recalled Item: Cookie Dough Ice Cream packed under the following brand names Recalled by...

The Issue: The Chocolate Chip Cookie Dough pieces in the ice cream have the potential...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 11, 2016· Roland Foods, LLC.

Recalled Item: Roland¿ Preserved Lemons Recalled by Roland Foods, LLC. Due to Undeclared...

The Issue: The product contains undeclared sulfites based on sampling and analysis by...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2016· Rosa Foods HQ

Recalled Item: Soylent Food Bars Recalled by Rosa Foods HQ Due to Rosa Foods is recalling...

The Issue: Rosa Foods is recalling Soylent Bar because a number of their customers have...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to St Jude Medical is...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to St Jude Medical is recalling...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Fortify VR Recalled by St Jude Medical Inc. Due to St Jude Medical is...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Advia Chemistry Calibrator For in vitro diagnostic use in the Recalled by...

The Issue: Siemens has confirmed that the DBIL_2 Assigned Calibrator Values (ACV)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Large Craniotome 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Electronic Foot Control with Direction or Irrigation Switches Product Usage:...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Autolube-III with NK 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.

Class II — Potential Health HazardOngoing