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. 2,492 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,492 in last 12 months

Showing 1346113480 of 48,376 recalls

DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree sample boxes Recalled by Dental Alliance Holdings LLC Due to...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 Recalled by Dental...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx21 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx36 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx26 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Akorn, Inc.

Recalled Item: Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles...

The Issue: Labeling: Missing Label

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Akorn, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Akorn, Inc. Due to...

The Issue: Labeling: Missing Label

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Gilead Sciences, Inc.

Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: investigation into a customer complaint...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 3, 2021· Slayer Forever, LLC dba BUBS Naturals

Recalled Item: BUBS Naturals Fountain of Youth Formula Recalled by Slayer Forever, LLC dba...

The Issue: Supplement contains undeclared milk from MCT oil powder ingredient.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 3, 2021· Wright Medical Technology Inc

Recalled Item: Stryker DARCO Screw Recalled by Wright Medical Technology Inc Due to The...

The Issue: The incorrect product is contained in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2021· Konica Minolta Healthcare Americas, Inc.

Recalled Item: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing...

The Issue: lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2021· Wright Medical Technology Inc

Recalled Item: Stryker CLAW II ORTHOLOC 3DSi Plate Recalled by Wright Medical Technology...

The Issue: The incorrect product is contained in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2021· Wright Medical Technology, Inc.

Recalled Item: Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw Recalled by Wright...

The Issue: Incorrect product is contained in the packaging.

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2021· Torrent Pharma Inc.

Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2021· LivaNova USA, Inc.

Recalled Item: Vagus Nerve Stimulation (VNS) Therapy Leads Recalled by LivaNova USA, Inc....

The Issue: A manufacturing issue may cause the silicone tubing wall thickness of vagus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2021· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: IPELA FHD PTZ TILE KITS with Axis cameras used in Recalled by Natus...

The Issue: Tile kits that allow one to install and situate a video camera within a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2021· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Veradius Unity Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Firm discovered that the wireless foot switch can suddenly stop responding...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2021· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Firm...

The Issue: Firm discovered that the wireless foot switch can suddenly stop responding...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2021· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Firm...

The Issue: Firm discovered that the wireless foot switch can suddenly stop responding...

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

Class II — Potential Health HazardOngoing