State

West Virginia product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7801–7825 of 76533

HighFDA (Drugs)·D-0219-2025·2025-02-12
Hydralazine Hydrochloride Tablets Recalled Due to Impurities and Degradation
SKY Packaging recalls Hydralazine Hydrochloride 25 mg tablets nationwide due to failed quality specifications for impurities and degradation.
Product
HydrALAZINE Hydrochloride, 25 mg, 100 Unit Dose Tablets (10x10), USP, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-327-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0480-2025·2025-02-12
French Crullers Recalled Nationwide for Potential Listeria Contamination
FGF, LLC is recalling French Crullers sold nationwide and in Canada due to potential Listeria monocytogenes contamination. All product with expiration dates from 12/13/24 and earlier is affected.
Product
item 8201812 FRENCH CRULLERS 72x 1.6 OZ, NET WT 6.48 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0481-2025·2025-02-12
FGF Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling dual-filled chocolate and Bavarian yeast ring donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed in the US and Canada.
Product
item 8201813 DUAL FILLED NATURALLY & ARTIFICIALLY FLAVORED CHOCOLATE AND BAVARIAN FILLED YEAST RING DONUT 80x3.1OZ, NET WT 13.97 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1072-2025·2025-02-12
VNS Therapy Generators May Stop Delivering Stimulation Due to Component Failure
The SenTiva and SenTiva Duo vagus nerve stimulation generators may stop delivering therapy due to an internal mechanical component becoming stuck, causing potential loss of seizure and depression control.
Product
SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve Stimulation (VNS).
Category
Medical Device
Distribution
41 states
HighFDA (Food)·F-0511-2025·2025-02-12
French Crullers Recalled for Potential Listeria Contamination
FGF, LLC is recalling JUST BAKED FRENCH CRULLERS nationwide due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Product
item 8201882 JUST BAKED FRENCH CRULLERS 96x1.6 OZ, NET WT 9.60 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0492-2025·2025-02-12
FGF Frozen Bismark Donuts Recalled Due to Listeria Contamination Risk
FGF, LLC is recalling frozen Bismark donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201843 GEN BISMARK DONUT DGH FRZ 144x2OZ, NET WT 16.20 LB
Category
Food
Distribution
Distributed nationwide
HighNHTSA·25V081000·2025-02-12
Volkswagen Atlas transmissions may have been manufactured incorrectly
Volkswagen is recalling certain 2025 Atlas and Atlas Cross Sport vehicles because the transmission may have been manufactured incorrectly, which can result in a loss of drive power.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V079000·2025-02-12
Porsche Recalls 2025 911 Models Due to Headlight Glare Software Error
Porsche is recalling 878 2025 911 vehicles because a software error causes low beam headlights to create excessive glare for oncoming traffic, increasing crash risk.
Product
PORSCHE — PORSCHE 911
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1114-2025·2025-02-12
Endodontic Files Recalled for Excess Irradiation Causing Package Integrity Issues
US Endodontics is recalling endodontic files due to irradiation above specification, which may compromise package integrity. The recall affects 789,729 devices distributed in the US and internationally.
Product
Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK AP120253PK AP120313PK AP125213PK AP125253PK AP125313PK AP135213PK AP135253PK AP135313PK AP145213PK AP145253PK AP145313PK AP1GP213PK AP1GP253PK AP1GP313PK O.U.S. Products: EdgeFile X7 REF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1093-2025·2025-02-12
Philips Azurion patient tables recalled for finger entrapment risk
Philips is recalling Azurion 7 M12 and Allura patient tables used in medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel may suffer finger injury if fingers are caught between the tabletop and guiding rails.
Product
Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1045-2025·2025-02-12
GE Discovery XR656 HD X-ray system AEC control malfunctions during imaging
GE Medical Systems is recalling the Discovery XR656 HD X-ray imaging system due to a malfunction in the Automatic Exposure Control (AEC) feature. The defect allows continued X-ray exposure beyond intended limits without requiring operator acknowledgment.
Product
Discovery XR656 HD. X-Ray imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1089-2025·2025-02-12
Philips Azurion 5 M12 imaging system: finger entrapment risk during tabletop repositioning
Philips Azurion 5 M12 patient imaging systems pose a finger entrapment hazard during manual tabletop repositioning. Operators and service personnel risk finger injury from the longitudinal guiding rails.
Product
Azurion 5 M12 System Code: (1) 722227 (2) 722231
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0510-2025·2025-02-12
FGF Donuts Recalled Nationwide Due to Listeria Contamination Risk
FGF ring donuts recalled nationwide for potential Listeria monocytogenes contamination. The recall covers 2,017,614 cases produced through December 13, 2024.
Product
item 8201879 RING RND DONUT ZGT PDF 96x2.25 OZ, NET WT 12.15 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0507-2025·2025-02-12
ESL Cinnamon Fries Recalled for Potential Listeria Contamination
ESL Cinnamon Fries (item 8201871) produced on December 13, 2024 and prior are being recalled due to potential contamination with Listeria monocytogenes. Approximately 2 million cases were distributed nationwide in the US and Canada.
Product
item 8201871 ESL CINNAMON FRIES 60x3OZ, NET WT 10.13 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0509-2025·2025-02-12
Pumpkin-shaped donuts recalled for potential Listeria contamination
FGF, LLC is recalling pumpkin-shaped donuts distributed nationwide due to potential contamination with Listeria monocytogenes. Consumers should not consume the product.
Product
item 8201876 PMPKN SHAPE DONUT ZGT PFD 84x1.75OZ, NET WT 8.27 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0471-2025·2025-02-12
Chocolate Donut Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling chocolate-coated donut rings nationwide due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases are affected. No illnesses have been reported.
Product
item 8201780 GEN CHOC CK DONUT RINGS PFD 90x2.5OZ, NET WT12.66LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0490-2025·2025-02-12
Frozen Persian Donuts Recalled Due to Listeria Contamination Risk
FGF, LLC is recalling frozen Persian donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Product
item 8201841 GEN PERSIAN DONUT DGH FRZ 168x2OZ, NET WT 18.90 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1085-2025·2025-02-12
Finger entrapment hazard in Philips Allura fluoroscopy patient tables
Philips is recalling AD7 and AD7X patient tables from Allura and Azurion fluoroscopy systems. During manual repositioning, fingers can become trapped between the guiding rails and tabletop, potentially causing injury.
Product
Allura Xper FD20/20 System Code: (1) 722038
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1118-2025·2025-02-12
Spine Surgery Planning Software Calculation Errors in Rod Planning Parameters
Medicrea International is recalling UNiD Spine Analyzer software due to calculation errors in rod planning parameters. The software experienced anomalies resulting in incorrect values for surgical classification and measurement parameters used in spine surgery planning.
Product
UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286929 Two cloud-based software applications within UNiD Adaptive Spine Intelligence (ASI): the UNiD HUB and the UNiD Spine Analyzer. The UNiD HUB cloud-based software is a he
Category
Medical Device
Distribution
50 states
HighFDA (Food)·F-0515-2025·2025-02-12
Apple Fritter Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling apple fritter donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Product
item 8201900 APPLE FRITTER DONUT ZGT PFD 54x3OZ, NET WT 9.11 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0479-2025·2025-02-12
Sour Cream Cake Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling Old Fashioned Sour Cream Cake Donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201811 OLD FASHIONED NATURALLY AND ARTIFICIALLY FLAVORED SOUR CREAM CAKE DONUTS 90x2.5 OZ, NET WT 12.66 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0508-2025·2025-02-12
FGF LLC Frozen Donuts Recalled for Listeria Contamination Risk
FGF, LLC is recalling BAV CRM BISMARK DONUT frozen donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not eat the product.
Product
item 8201872 BAV CRM BISMARK DONUT PFD 60x3.85OZ, NET WT 12.99 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0482-2025·2025-02-12
Bavarian Paczki Recalled for Listeria Monocytogenes Contamination Risk
FGF, LLC is recalling Bavarian Paczki (item 8201814) due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201814 BAVARIAN PACZKI 66x4OZ, NET WT 14.85 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1086-2025·2025-02-12
Philips AD7 and AD7X Patient Table Finger Entrapment Risk
The Philips AD7 and AD7X patient tables pose a finger entrapment risk during manual repositioning. Operators and service personnel could sustain finger injuries from the gap between the longitudinal guiding rails and tabletop.
Product
AlluraXperFD20/15 System Code: (1) 722058
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1080-2025·2025-02-12
Philips recalls AlluraXper FD20 patient tables due to finger entrapment hazard
Philips is recalling AlluraXper FD20 patient tables due to a finger entrapment hazard. During manual repositioning, fingers can get trapped between the tabletop and rails, risking injury to operators and service personnel.
Product
AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028
Category
Medical Device
Distribution
Distributed nationwide