State

West Virginia product recalls

72,984 recalls have nationwide distribution and so reach West Virginia. 3,541 additional recalls listed West Virginia specifically in their distribution scope.

What the numbers show

Total: 3,541
Critical: 593
Severe: 657
Most recent: 2026-09-09

Of the 3,541 recalls naming West Virginia we have scored against our rubric, 593 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 657 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,541 recalls whose distribution notice names West Virginia specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6426–6450 of 76525

HighCPSC·25324·2025-06-05
Direct Scaffold Supply Baker Scaffolding Casters Recalled for Fall Hazard
Direct Scaffold Supply is recalling casters used in multi-purpose baker style scaffolding due to faulty spot welds that can cause caster failure and scaffolding instability, creating a fall hazard. One injury from a caster failure has been reported.
Product
Casters on Direct Scaffold Supply Multi-Purpose Baker Style Scaffolding Products
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25314·2025-06-05
Hobby Toy Hammer Ball Sets Recalled for Choking Hazard Risk
Hobby Toy Hammer Ball sets sold on Amazon contain small balls that violate federal toy safety regulations for children under three and pose a choking hazard. About 2,000 units sold from September 2024 through April 2025 are affected.
Product
Hobby Toy Hammer Ball sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25321·2025-06-05
Yamaha Golf Car Vehicles Recalled Due to Accelerator Pedal Spring Failure
Yamaha is expanding a recall of approximately 352,000 golf car vehicles because the accelerator pedal spring can fail to return to idle, posing a crash hazard. No injuries have been reported to date.
Product
Yamaha Golf Car Vehicles
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25313·2025-06-05
Rinnai i-Series Plus Gas Boilers Recalled for Carbon Monoxide Hazard
Rinnai America is recalling about 2,030 i-Series Plus gas boilers because the door can fail to seal properly due to incorrect screws, allowing carbon monoxide to escape. No injuries have been reported.
Product
Rinnai i-Series Plus gas boilers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25319·2025-06-05
Specialized Globe-Branded Haul ST and LT E-Bikes Recalled for Fall Hazard
Specialized Bicycle Components is recalling about 11,100 Globe-branded Haul ST and LT e-bikes due to a telescopic seat post that can break when fully extended, creating a fall hazard. The company has received 13 incident reports including two minor injuries.
Product
Haul ST and LT E-bikes with telescopic seat posts
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·25317·2025-06-05
Lutron Power Interfaces for LED Tape Lights Recalled for Shock Hazard
Lutron-branded power interfaces for LED tape lights can fail during power surges like lightning strikes, creating a shock hazard. About 1,944 units are affected; no injuries have been reported.
Product
Lutron-branded power interfaces for LED tape lights
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1818-2025·2025-06-04
ELEOS Collar Stem 15mm mistakenly labeled as 13mm modular stem
Onkos Surgical is recalling ELEOS Collar Stem components (Model HC-15120-03M) that were packaged and labeled as 13mm modular segmental stems when they are actually 15mm in diameter. This mislabeling could result in implantation of an incorrectly-sized component during limb salvage surgery.
Product
ELEOS COLLAR STEM, CEMENTED, FLUTED, 15MM X 120MM. Model Number: HC-15120-03M. Component of Limb Salvage System with BioGrip.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0448-2025·2025-06-04
Carvedilol Tablets Recalled Due to N-Nitroso Impurity
Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 3.125mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit. The recall affects 100-count and 500-count bottles distributed nationwide.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V374000·2025-06-04
Triple E Recalls 2025 Motorhomes Due to Wiring Insulation Defect
Triple E is recalling 2025 Wonder and Unity motorhomes because incorrectly installed inverter wiring insulation may overheat, increasing the risk of fire.
Product
TRIPLE E RV — TRIPLE E RV, TRIPLE E WONDER, UNITY
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1817-2025·2025-06-04
ELEOS Collar Stem Cemented Fluted Implant Size Mislabeling Recall
Onkos Surgical is recalling 23 units of ELEOS Collar Stem implants (Model HC-13120-03M) because packages labeled as 13mm contained 15mm diameter implants instead, creating a risk of implant mismatch during surgery.
Product
ELEOS COLLAR STEM, CEMENTED, FLUTED, 13MM X 120MM. Model Number: HC-13120-03M. Component of Limb Salvage System with BioGrip.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0453-2025·2025-06-04
Endurance Boost With Horny Goat Weed Supplement Recalled for Undisclosed Drug Content
VEPEMVA Nutrition's Endurance Boost with Horny Goat Weed has been recalled because it contains Sildenafil and Propoxyphenylsildenafil, undisclosed active pharmaceutical ingredients. The product was marketed and sold without FDA approval.
Product
ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0449-2025·2025-06-04
Carvedilol Tablets 6.25 mg Recalled for N-Nitroso Impurity
Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 6.25 mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit. The recall affects 100-count and 500-count bottles distributed nationwide.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0451-2025·2025-06-04
Carvedilol Tablets 25 mg Recalled Due to Impurity Above Acceptable Limit
Glenmark Pharmaceuticals is recalling Carvedilol Tablets USP 25 mg nationwide due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit, resulting from CGMP deviations.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0450-2025·2025-06-04
Carvedilol Tablets 12.5 mg Recalled for Impurity Above Limit
Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 12.5 mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit, resulting from current Good Manufacturing Practice (CGMP) deviations.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1874-2025·2025-06-04
Umbilical Vessel Catheter 5 French Dual Lumen Packaging Defect Recall
Cardinal Health is recalling umbilical vessel catheters due to a packaging defect that may compromise product sterility. Use of non-sterile catheters could lead to infection in neonates.
Product
Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual lumen
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1870-2025·2025-06-04
Cardinal Health Umbilical Vessel Catheter Insertion Tray Recall
Cardinal Health is recalling one lot of umbilical vessel catheter insertion trays due to a packaging defect that may compromise sterility. Use of a non-sterile product on neonates could lead to infection.
Product
Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1860-2025·2025-06-04
DORO Easy-Connect Navigation Adaptor compatibility issue recall
Pro-Med Instruments is recalling the DORO Easy-Connect Navigation Adaptor due to potential compatibility problems that could affect positioning accuracy and navigation system function. The company distributed 217 units worldwide.
Product
DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1848-2025·2025-06-04
Abbott Diagnostics Vitamin D Calibrator Transit Storage Conditions Issue
The Abbott Diagnostics Architect Vitamin D 6-Level Calibrator was exposed to improper storage conditions during transit due to severe thunderstorms, which may result in incorrect or delayed test results.
Product
ABBOTT DIAGNOSTICS ARCHITECT VITAMIND 6LEVEL CALIBRATOR.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1873-2025·2025-06-04
Umbilical Vessel Catheter 5 French Single Lumen Packaging Defect Recall
Cardinal Health is recalling umbilical vessel catheters due to a packaging defect that may compromise sterility, risking infection in newborns if non-sterile products are used.
Product
Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1864-2025·2025-06-04
NxStage PureFlow-B Solution Bags Perimeter Seal Failure Risk
NxStage Medical Inc is recalling NxStage PureFlow-B Solution bags nationwide due to potential perimeter seal failure on the small chamber, which could cause electrolyte fluid to splash into the user's face when opening the peel seam to mix chambers before treatment.
Product
NxStage PureFlow-B Solution. Catalog numbers: RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-406, RFP-453, RFP-454, RFP-456.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1833-2025·2025-06-04
Ortho Clinical Diagnostics Vancomycin Reagent Cold Chain Recall
Mckesson Medical-Surgical is recalling Ortho Clinical Diagnostics Vancomycin reagent (Catalog No. 6801709) distributed nationwide due to transit delays and severe thunderstorms that may have caused storage outside recommended conditions, risking incorrect or delayed test results.
Product
ORTHO CLINICAL DIAGNOSTICS INC VANCOMYCIN (300/BX)ORCLNL REAGENT.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1850-2025·2025-06-04
Abbott Diagnostics Architect Free T4 Calibrator Recall
Abbott Diagnostics Architect Free T4 Calibrator units may have been exposed to improper storage conditions due to transit delays from severe thunderstorms, potentially causing incorrect or delayed test results.
Product
ABBOTT DIAGNOSTICS ARCHITECT FREE T4ABBDIA CALIBRATOR.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1871-2025·2025-06-04
Cardinal Health Umbilical Vessel Catheter Recall for Sterility Defect
Cardinal Health is recalling 1,710 units of Umbilical Vessel Catheter 2.5 French single lumen due to a packaging defect that may compromise sterility. Non-sterile catheters could cause infection in neonates.
Product
Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1849-2025·2025-06-04
Abbott Diagnostics Architect Total T36X4ML Calibrator Cold Chain Excursion
Abbott Diagnostics Architect Total T36X4ML Calibrator units experienced transit delays during severe thunderstorms that may have caused storage outside recommended temperature conditions, potentially resulting in incorrect or delayed test results.
Product
ABBOTT DIAGNOSTICS ARCHITECT TOTAL T36X4ML CALIBRATOR.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V324000·2025-06-04
2025 Nissan Frontier rear display may blank in reverse
The 2025 Nissan Frontier's center information display may show a blank screen in reverse, violating federal rear-visibility standards. This could reduce driver visibility and increase crash risk.
Product
NISSAN — NISSAN FRONTIER, KICKS
Category
Vehicle
Distribution
Distributed nationwide