State

West Virginia product recalls

73,206 recalls have nationwide distribution and so reach West Virginia. 3,570 additional recalls listed West Virginia specifically in their distribution scope.

What the numbers show

Total: 3,570
Critical: 603
Severe: 669
Most recent: 2026-09-23

Of the 3,570 recalls naming West Virginia we have scored against our rubric, 603 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 669 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,570 recalls whose distribution notice names West Virginia specifically. The 73,206 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12801–12825 of 76776

SevereFDA (Drugs)·D-0346-2024·2024-02-28
TING Athlete's Foot Spray Recalled Due to Benzene Contamination
Insight Pharmaceuticals is recalling TING 1% Tolnaftate Athlete's Foot Spray due to benzene contamination. The recall affects approximately 59,644 cans distributed nationwide.
Product
TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591 UPC 3 63736 81961 3
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0345-2024·2024-02-28
Dietary supplement Arize recalled for undeclared pharmaceutical ingredient
Arize Herbal Dietary Supplement contains an undeclared ingredient (nortadalafil), a pharmaceutical used in FDA-approved male sexual enhancement medications, making it an unapproved drug.
Product
Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001, www.getarize.com
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0334-2024·2024-02-28
Drug Recalled for Marketing Unapproved Tianeptine Without FDA Approval
Neptune's Fix Tianeptine Elixir is recalled nationwide for containing tianeptine, an FDA-unapproved substance. The product was marketed without required FDA approval.
Product
Neptune's Fix, Tianeptine Extra Strength Elixir, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0344-2024·2024-02-28
SCHWINNNG Herbal Dietary Supplement Recalled for Undeclared Nortadalafil Content
SCHWINNNG Herbal Dietary Supplement (Lot #2108, exp. 10/31/2024) is recalled nationwide because it contains undeclared nortadalafil, an active pharmaceutical ingredient used for male sexual enhancement. The FDA classified this as an unapproved drug.
Product
SCHWINNNG Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Today the World LLC, Vancouver, WA 98683
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V155000·2024-02-28
Porsche Recalls 2020-2024 911 Models for Windshield and Rear Window Defects
Porsche is recalling 2020-2024 911 vehicles because the front windshield and rear window may not be properly secured and can detach, increasing injury risk during air bag deployment.
Product
PORSCHE — PORSCHE 911
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0343-2024·2024-02-28
Herbal dietary supplement recalled for undeclared drug ingredient
Sustain Herbal Dietary Supplement is being recalled nationwide for containing undeclared tadalafil, a pharmaceutical ingredient. The product was marketed as a dietary supplement but contains an unapproved drug.
Product
Sustain Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by VSD Productions, Inc. Las Vegas, Nevada
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0333-2024·2024-02-28
FDA Recalls Neptune's Fix Tianeptine Elixir for Containing Unapproved Drug
Neptune's Fix Tianeptine Elixir has been recalled because it contains tianeptine, an unapproved drug substance in the United States. Approximately 1 million bottles distributed nationwide are affected.
Product
Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V156000·2024-02-28
Nissan Rogue seat belt pretensioners may not restrain occupants properly
Nissan is recalling certain 2023 Rogue vehicles because incorrectly manufactured driver and front passenger seat belt pretensioners may fail to restrain occupants, breaching FMVSS 208, 209 and 210.
Product
NISSAN — NISSAN ROGUE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0335-2024·2024-02-28
Neptune's Fix Tianeptine Tablets Recalled for FDA Unapproved Marketing
Neptune's Fix Tianeptine Tablets are being recalled because the product contains tianeptine, a substance not approved by the FDA for any medical use. The recall affects 4,932 boxes distributed nationwide.
Product
Neptune's Fix, Tianeptine Tablets Extended Relief, Twenty Tablets per Box, Wide Awake, 3000 mg (150 mg Per Tablet), Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V158000·2024-02-28
Jayco Recalls 2024 Motorhomes Due to Rear Axle Lubricant Defect
Jayco is recalling 2024 Entegra and Jayco motorhomes because inadequate rear axle lubricant may cause bearing damage, leading to wheel lock-up or driveshaft separation.
Product
ENTEGRA — ENTEGRA, JAYCO CONDOR, SOLSTICE, EXPANSE LI, EXPANSE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0328-2024·2024-02-28
CVS Health Cherry Cough Drops recalled for potential glass and silicone particles
Bestco LLC is recalling CVS Health Cherry Cough Drops nationwide due to potential glass and silicone particulates resulting from manufacturing process deviations.
Product
CVS Health Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 160 drops per bag, item number 20001089, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0330-2024·2024-02-28
Kroger Cherry Cough Drops recalled for potential glass and silicone contamination
Bestco LLC is recalling Kroger Cherry Cough Drops due to potential glass and silicone particulates in the product. The recall affects product distributed nationwide.
Product
Kroger Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000064, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1146-2024·2024-02-28
Henry Schein Criterion Level 3 Earloop Masks Recalled for Non-Validated Equipment
AMD Medicom Inc. is recalling Henry Schein Criterion Level 3 Earloop Masks because they were produced on non-validated equipment not included in the initial product qualification.
Product
HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0340-2024·2024-02-28
Prescription injection drug recalled due to temperature excursion during shipment
Acthar Gel (repository corticotropin injection) is being recalled due to a temperature excursion during shipping from the manufacturer to distributor. Lot #1564-103 should not be dispensed to patients.
Product
ACTHAR — ACTHAR (REPOSITORY CORTICOTROPIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1171-2024·2024-02-28
Cardiology imaging software may calculate heart chamber size incorrectly
Synapse Cardiology PACS software versions 7.0–7.3.0 may calculate left ventricle mass incorrectly, potentially leading to misdiagnosis or wrong treatment plans. Thirteen units have been distributed in the US and Israel.
Product
Synapse Cardiology PACS V7.3.0, V7.2, V7.1, V7.0. A web-based application as the primary user interface for the processing of medical images.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1174-2024·2024-02-28
Aquabiliti saline flush syringes recalled for potential sodium chloride content deficiency
MRP, LLC is recalling AQUABILITI AQUASTAT saline flush syringes because they may fail to meet USP standards for sodium chloride content after 12 months.
Product
AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe, USP, 5mL in 12mL, REF 2T0805; and 3mL in 12mL, REF 2T0807, intermediate cartons containing 100 syringes, shipping cases containing 400 syringes, Rx, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0326-2024·2024-02-28
Fluticasone Propionate Nasal Spray Recalled for Potential Bacterial Contamination
Apotex Corp. is recalling Fluticasone Propionate Nasal Spray (292,752 bottles nationwide) due to potential Burkholderia cepacia contamination from manufacturing deviations. No illnesses reported.
Product
FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0339-2024·2024-02-28
Fosfomycin Tromethamine Granules Recalled for Out-of-Specification Organic Impurities
Ascend Laboratories recalls 71,244 sachets of Fosfomycin Tromethamine for failing quality specifications due to organic impurities. Patients with affected lots should consult their healthcare provider.
Product
FOSFOMYCIN TROMETHAMINE — FOSFOMYCIN TROMETHAMINE (FOSFOMYCIN TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1150-2024·2024-02-28
Epidural Tray Kits Recalled for Wrong Connector Type
B. Braun Medical recalls 3,890 PERIFIX epidural trays nationwide due to filter straws with incompatible neuraxial connectors instead of standard Luer connectors.
Product
Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, 5 mL Glass Luer Lock LOR Tray (Kit) A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management of pain. It includes the pharmaceutical…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1151-2024·2024-02-28
Philips Allura Xper X-ray systems disk bay component may malfunction
Philips has recalled certain Allura Xper interventional X-ray systems because the disk bay component may fail, potentially preventing system operation and imaging procedures.
Product
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: Imaging Processing PC, Host PC, FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1179-2024·2024-02-28
Biliary Endoprosthesis Labeling Mismatch Risks Incorrect Device Placement
W.L. Gore's GORE VIABIL Short Wire Biliary Endoprosthesis may be mislabeled regarding drainage holes, risking extended procedures, infections, and unplanned device removal in 24 units distributed in Georgia.
Product
GORE VIABIL Short Wire Biliary Endoprosthesis, Product labeled as (1) Catalog Number VSWVH1008, 10 mm x 8 cm; with holes; and (2) Catalog Number VSWVN1008, 10 mm x 8 cm; no holes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1149-2024·2024-02-28
PERIFIX epidural kits recalled for incompatible filter straw connectors
B. Braun PERIFIX epidural kits contain filter straws with Neuraxial connectors instead of Standard Luer Connections, preventing proper assembly of the kits.
Product
Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, PERIFIX FX 19 Ga. Springwound Closed Tip Catheter, 5 mL Glass Luer Lock LOR Tray (Kit)-A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1177-2024·2024-02-28
Azurion 5 X-Ray System Generator May Fail Due to Circuit Short
Philips Azurion 5 X-ray systems with Certeray generators may experience power loss due to a potential short circuit in the power inverter board, potentially delaying or interrupting medical procedures.
Product
Azurion 5 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722227 (2) 722228
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1144-2024·2024-02-28
Philips Allura Xper Interventional X-ray System Display and Imaging Malfunction
A framegrabber card malfunction in Philips Allura Xper interventional X-ray systems may cause display failures, preventing proper visualization of medical images and delaying procedures.
Product
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10/10 722005…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1147-2024·2024-02-28
Henry Schein Criterion Anti-Fog Earloop Masks Recalled for Equipment Validation Issue
AMD Medicom Inc. is recalling Henry Schein Criterion Anti-Fog Earloop Masks Level 3 (Blue) because the masks were produced on non-validated equipment not included in the product qualification process.
Product
HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-3281)
Category
Medical Device
Distribution
Distributed nationwide