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.

7776–7800 of 76533

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-0499-2025·2025-02-12
FGF Sour Cream Cake Donuts Recalled Due to Listeria Contamination Risk
FGF's Just Baked Sour Cream Cake Donuts are being recalled nationwide due to potential Listeria monocytogenes contamination. Approximately 2 million cases produced on or before December 13, 2024 are affected.
Product
item 8201860 JUST BAKED SOUR CREAM CAKE DONUTS 120x2.5 OZ, NET WT 18.75 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0473-2025·2025-02-12
Apple fritter recall due to potential Listeria monocytogenes contamination
FGF LLC is recalling apple fritters nationwide due to potential Listeria monocytogenes contamination. All product produced on or before December 13, 2024 is affected.
Product
item 8201805 APPLE FRITTER 60x2.5 OZ, NET WT 8.44 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0477-2025·2025-02-12
FGF Plain Cake Donuts Recalled Due to Potential Listeria Contamination
FGF, LLC is recalling 2,017,614 cases of plain cake donuts distributed nationwide in the US and Canada due to potential contamination with Listeria monocytogenes. No illnesses have been reported.
Product
item 8201809 PLAIN CAKE DONUT 108x2.25 OZ, NET WT 13.67 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0474-2025·2025-02-12
Raspberry-filled donuts recalled for potential Listeria monocytogenes contamination
FGF, LLC is recalling raspberry-filled donuts nationwide due to potential Listeria monocytogenes contamination. The recall affects donuts produced through 12/13/24.
Product
item 8201806 RASPBERRY FILLED DONUT 78x2.75OZ, NET WT 12.07 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0528-2025·2025-02-12
Unfilled Bismarck Donuts Recalled Due to Listeria Contamination Risk
FGF, LLC is recalling over 2 million cases of unfilled Bismarck donuts due to potential Listeria monocytogenes contamination. The recall affects products distributed nationwide in the US and Canada.
Product
item 8202731 UNFLD BISMARK DONUT PFD 78X3OZ, NET WT 13.16 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0522-2025·2025-02-12
French Cruller Recall Due to Listeria Contamination Risk
FGF, LLC is recalling French Crullers (item 8201921) distributed nationwide in the US and Canada due to potential Listeria monocytogenes contamination.
Product
item 8201921 FRENCH CRULLER PFD 72x1.6 OZ, NET WT 6.48 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0472-2025·2025-02-12
FGF Yeast Ring Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling 2,017,614 cases of yeast ring donuts nationwide due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024.
Product
item 8201804 Yeast Ring Donut 108x2.15OZ, NET WT 13.06 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0478-2025·2025-02-12
Fluff Bars Recalled Due to Potential Listeria Monocytogenes Contamination
FGF, LLC is recalling item 8201810 Fluff Bars distributed nationwide to the US and Canada due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Product
item 8201810 FLUFF BAR 78x2.75 OZ, NET WT 12.07 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0493-2025·2025-02-12
Frozen Persian Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling frozen Persian donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201844 GEN GLD PERSIAN DONUT DGH FRZ 132x2.5OZ, NET WT 18.56 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0520-2025·2025-02-12
Yeast Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling yeast donuts nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.
Product
item 8201919 BAR YST DONUT UNFLD PFD 74x3OZ, NET WT 12.49 LB
Category
Food
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
HighNHTSA·25V080000·2025-02-12
Audi Q5 and A7 high voltage batteries may overheat
Volkswagen is recalling certain 2021-2024 Audi Q5 and 2022 A7 e plug-in hybrid vehicles because the high-voltage battery may overheat, increasing the risk of a fire.
Product
AUDI — AUDI Q5, A7 E
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1087-2025·2025-02-12
Philips Azurion and Allura Patient Tables: Finger Entrapment Hazard
Philips patient tables on Azurion and Allura imaging systems can trap fingers between the tabletop and rails during manual repositioning. Operators and service personnel are at risk of finger injury.
Product
Azurion 3 M12 System Code: (1) 722063 (2) 722221
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1083-2025·2025-02-12
Philips AlluraXper Operating Room Table Finger Entrapment Hazard
The Philips AlluraXper FD20 operating room table can trap fingers between the guiding rails and tabletop during manual repositioning, potentially injuring operators and service personnel.
Product
AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1084-2025·2025-02-12
Philips Allura and Azurion Patient Tables Recall Due to Finger Entrapment Risk
Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel are at risk of finger injury.
Product
AlluraXperFD20/10 System Code: (1) 722029
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1091-2025·2025-02-12
Philips Azurion and Allura System Patient Tables: Finger Entrapment Risk
Philips Azurion and Allura system patient tables may trap fingers between the guiding rails and tabletop during manual repositioning, risking finger injury to operators and service personnel.
Product
Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1099-2025·2025-02-12
Belmont Medical 3-Spike Disposable Set May Leak During Use
The Belmont Medical 3-Spike Disposable Set may leak during priming due to a crack in its female quick connector, potentially delaying warmed infusions in hospital settings.
Product
Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Infuser RI-2. Designed to be used in general operation in hospital or alternate care environments to provide warmed blood and fluids to any patients e10 kg requiring warmed infusion. Part Number:903-00006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0476-2025·2025-02-12
FGF LLC Persian Donut Recalled for Potential Listeria Contamination
FGF LLC is recalling Persian Donut item 8201808 nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should discard it or return it to the retailer.
Product
item 8201808 PERSIAN DONUT 78x2.25 OZ, NET WT 9.87 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1043-2025·2025-02-12
X-Ray imaging systems may allow radiation exposure beyond safety limits
GE Medical Systems is recalling Definium 656HD and Discovery XR656HD X-Ray systems due to an Automatic Exposure Control defect that may allow radiation exposure to exceed intended safety limits.
Product
Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226, 00840682136709). X-Ray imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0220-2025·2025-02-12
HydrALAZINE Hydrochloride tablets recalled for failed purity and degradation specifications
SKY PACKAGING is recalling HydrALAZINE Hydrochloride 50mg tablets nationwide due to failed impurities and degradation specifications. Four affected lot numbers have expiration dates from April 2025 to February 2026.
Product
HydrALAZINE Hydrochloride, 100 Tablets (10x10), USP, 50mg, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-328-10
Category
Drug
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-1076-2025·2025-02-12
Philips Allura CV20 patient tables risk finger entrapment during repositioning
The Philips Allura CV20 System patient tables (AD7 and AD7X models) pose a finger entrapment hazard during manual repositioning. Fingers can become caught between the tabletop and guiding rails, potentially injuring operators and service personnel.
Product
Allura CV20 System Code: 722031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1088-2025·2025-02-12
Philips Azurion Patient Tables Recalled for Finger Entrapment Risk
Philips Azurion patient tables used in medical imaging systems can trap fingers between the tabletop and rails during manual repositioning, potentially causing finger injury to operators and service personnel.
Product
Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V078000·2025-02-12
Porsche Recalls 2023 911 Models Due to Rear Seat Belt Bolt Issue
Porsche is recalling 2023 911 vehicles because rear seat belt buckle bolts may not be tightened properly, which could reduce occupant restraint during a crash.
Product
PORSCHE — PORSCHE 911
Category
Vehicle
Distribution
Distributed nationwide