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. 2,356 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,356 in last 12 months

Showing 2758127600 of 48,376 recalls

DrugJuly 24, 2017· EZWeightLossTX LLC

Recalled Item: LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 24, 2017· EZWeightLossTX LLC

Recalled Item: LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 24, 2017· Teva Pharmaceuticals USA

Recalled Item: Famotidine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Tablet/Capsule Specification; out of specification for tablet weight

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2017· Chiavna Saffron LLC

Recalled Item: Super Panther 7K Capsules 1250 mg blend Recalled by Chiavna Saffron LLC Due...

The Issue: Marketed without an Approved NDA/ANDA;FDA analysis found product to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 21, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Implant Direct Swish Duo-Grip Healing Collar Recalled by Implant Direct...

The Issue: The Swish Duo-Grip Healing Collar part number 9048-13H (4.8mm) package...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2017· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: FUJINON ED-530XT. This device is intended for the visualization of Recalled...

The Issue: An update to the design and labeling was implemented to help reduce patient...

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

Class II — Potential Health HazardOngoing
FoodJuly 21, 2017· GRANDE PRODUCE LTD CO

Recalled Item: Caribena yellow maradol papaya packed in 35 pound cases Recalled by GRANDE...

The Issue: Product is contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 20, 2017· Grandma's Herbs

Recalled Item: "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT Recalled by...

The Issue: Grandmas Herbs Cholesterol has undeclared soy lecithin.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 20, 2017· Beckman Coulter Inc.

Recalled Item: Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K Recalled by Beckman...

The Issue: Reagent carryover from Sekisui ACTH when utilized on the BEC AU 680 analyzer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
DrugJuly 19, 2017· AVKARE Inc.

Recalled Item: Voriconazole Tablets Recalled by AVKARE Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out of specification for a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodJuly 19, 2017· TRULY GOOD FOODS

Recalled Item: Pumpkin Seeds Recalled by TRULY GOOD FOODS Due to Undeclared Allergen

The Issue: Undeclared allergen Tree Nuts: Blackened Seasoned Pumpkin Seeds mixed up...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Vyaire Medical

Recalled Item: AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER Recalled by Vyaire...

The Issue: Lot #0001047501 of the 9025RHTR ABG sampling kits have been manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...

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

Class II — Potential Health HazardOngoing