State

West Virginia product recalls

73,104 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 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10401–10425 of 76674

SevereFDA (Food)·F-1660-2024·2024-08-14
Patriotic Pretzel Products Recalled for Potential Salmonella Contamination
Palmer & Company is recalling Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists and Palmer Candy Frosted Patriotic Pretzels nationwide due to potential salmonella contamination.
Product
1. Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists, Net Wt 14 oz., UPC 78742 03913, 8/14oz case 2. Palmer Candy Frosted Patriotic Pretzels, Item 10757, Net Wt 28 lbs, UPC 77232 10757
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1659-2024·2024-08-14
Palmer Candy Cookies & Cream Yummy Chow Recalled for Salmonella Contamination Risk
Palmer & Company is recalling Palmer Candy Cookies & Cream Yummy Chow (Item 10706) nationwide due to potential salmonella contamination. Consumers should not consume the product.
Product
Palmer Candy Cookies & Cream Yummy Chow, Item 10706, Net Wt. 14 lbs, UPC 77232 10706
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1670-2024·2024-08-14
Peanut Butter Snack Mix Recalled for Potential Salmonella Contamination
Palmer & Company is recalling Freshness Guaranteed Peanut Butter Snack Mix due to potential salmonella contamination. The recall affects 12oz and 4.5oz packages distributed nationwide in the United States and Canada.
Product
1. Freshness Guaranteed Peanut Butter Snack Mix, Net Wt 12oz, UPC 78742 03912, 8/12oz case 2. Peanut Butter Snack Mix, Net Wt 4.5oz to go container, Distributed by: Kwik Trip Inc; UPC 39779 00424, 12/4.5oz case
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1663-2024·2024-08-14
Palmer Patriotic Munchy Medley Recalled for Potential Salmonella Contamination
Palmer & Company is recalling Palmer Patriotic Munchy Medley candy nationwide in the United States and Canada due to potential salmonella contamination.
Product
Palmer Patriotic Munchy Medley, Net Wt 15oz, UPC 7723237060, 12/15oz case
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1656-2024·2024-08-14
Yogurt-Covered Pretzel Recall Due to Potential Salmonella Contamination
Palmer & Company is recalling multiple yogurt-covered pretzel products distributed nationwide due to potential salmonella contamination. Consumers should not consume these products.
Product
1. Palmer Candy Classic Yogurt Pretzels, Net Wt 28 lbs, UPC 77232 10847 2. Sweet Smiles Yogurt Covered Pretzels, Net Wt. 3.25oz, UPC 77232 13641, 8/3.25oz case 3. Sconza Chocolates Yogurt Pretzels, Net Wt 14lbs, UPC 004166882015 4. Sunny Select Vanilla Yogurt Coated Pretzels…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1697-2024·2024-08-14
Wiers Farm Butternut Squash Recalled for Listeria Monocytogenes
Wiers Farm Inc is recalling Butternut Squash in 1-pound cartons due to potential Listeria monocytogenes contamination. Lot numbers 240705 through 240712 are affected.
Product
Wiers Farm - Butternut Squash packaged in 1lb cartons - case size dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1689-2024·2024-08-14
Green Bell Peppers Recalled for Listeria monocytogenes Contamination
Wiers Farm green bell peppers packaged in 1-pound cartons are being recalled due to potential Listeria monocytogenes contamination. Affected lot numbers are 240705 through 240712, distributed across 17 states.
Product
Wiers Farm - Green Bell Pepper packaged into 1lb carton - cases size dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1688-2024·2024-08-14
Wiers Farm Habanero Peppers Recalled for Listeria Contamination
Wiers Farm Inc is recalling habanero peppers sold in 1-pound cartons across 17 states due to potential Listeria monocytogenes contamination. The recall involves 441 cases with lot numbers 240705 through 240712.
Product
Wiers Farm - Habanero Peppers packaged into 1lb carton - 3lb per case
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1694-2024·2024-08-14
Wiers Farm Plain Parsley Recalled Due to Listeria Contamination
Wiers Farm Inc is recalling 148 cases of Plain Parsley due to potential Listeria monocytogenes contamination. The affected product was distributed across 17 states.
Product
Wiers Farm - Plain Parsley packaged in 1lb cartons - 15 cartons per case
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1680-2024·2024-08-14
Wiers Farm Serrano Peppers recalled for Listeria monocytogenes contamination
Wiers Farm Inc is recalling Serrano Peppers sold in 4oz bags due to potential Listeria monocytogenes contamination. The recall affects approximately 1,708 cases distributed across 16 states.
Product
Wiers Farm - Serrano Peppers packaged in 4oz plastic bag - 5lbs per case
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1684-2024·2024-08-14
Organic Zucchini Squash Recalled Due to Listeria Contamination
Wiers Farm is recalling organic zucchini squash due to potential Listeria monocytogenes contamination. The recall affects 337 cases across 17 states with lot numbers 240705 through 240712.
Product
Wiers Farm - Organic Zucchini Squash packaged into 2 count trays - cases dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1687-2024·2024-08-14
Cilantro Recalled Due to Listeria Monocytogenes Contamination
Wiers Farm is recalling cilantro packaged in 1-pound cartons due to potential Listeria monocytogenes contamination. The affected product was distributed to 2,798 cases across 16 U.S. states.
Product
Wiers Farm - Cilantro packaged into 1lb cartons - 30 or 60 cartons per case dependent on customer
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-2508-2024·2024-08-14
Philips IntelliVue Patient Monitor Software Missing Critical Entitlements
Philips IntelliVue Patient Monitor models with software L.x and M.x lack critical monitoring capabilities due to a software update. This could result in incorrect or delayed patient treatment.
Product
IntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866060. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0634-2024·2024-08-14
Gabapentin 600 mg Tablets Recalled Due to Metformin Contamination
Granules Pharmaceuticals Inc. is recalling Gabapentin Tablets 600 mg nationwide after fused Metformin ER tablets were found in bottles, creating a risk of unintended medication exposure.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2491-2024·2024-08-14
BD PYXIS MEDBANK Cabinet Software Causes Incorrect Medication Labels
FDA recall of BD PYXIS MEDBANK automated medication dispensing cabinets due to a software defect that prints incorrect bin information on restock labels, potentially leading to medication identification errors.
Product
BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P, REF: 169-85 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1648-2024·2024-08-14
Premo King Club Footlong Sandwiches Recalled for Potential Salmonella Contamination
Lipari Foods is recalling Premo King Club Footlong sandwiches (UPC 612510094259) due to potential Salmonella contamination. The recall affects 216 cases distributed to retailers across 16 states; consumers should discard the product or return it to the store.
Product
Premo King Club Footlong 11.5oz, clear plastic, UPC 612510094259, 4 retail packages per wholesale case
Category
Food
Distribution
16 states
HighFDA (Devices)·Z-2496-2024·2024-08-14
Automated Medication Dispensing Cabinet Software Issue with Incorrect Bin Labeling
BD PYXIS MEDBANK automated medication dispensing cabinets with software version 3.9.1.9 may generate incorrect bin location labels during restocking. This could cause medications to be placed in wrong storage locations.
Product
BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P, REF: 169-91 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V610000·2024-08-14
Holiday Rambler Admiral motorhomes recalled for missing GFCI outlet protection
Certain 2019-2025 Holiday Rambler Admiral and other RVs have exterior patio outlets lacking GFCI protection when powered by generator or shore cord, increasing electrical shock risk. Dealers will install GFCI devices free of charge.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, ADMIRAL, ECLIPSE, FLEX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1664-2024·2024-08-14
Palmer Patriotic White Fudge Cookies Recalled for Potential Salmonella
Palmer & Company is recalling Palmer Patriotic White Fudge Cookies in 7oz and 13.5oz sizes due to potential salmonella contamination. Affected products were distributed nationwide in the United States and Canada.
Product
1. Palmer Patriotic White Fudge Cookies, Net Wt. 7oz, UPC 7723237084, 16/7oz case 2. Palmer Patriotic White Fudge Cookies, Net Wt. 13.5 oz, UPC 7723237085, 8/13.5oz case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2534-2024·2024-08-14
Philips Azurion X-ray System: Potential Loss of Imaging Functionality
The Philips Azurion Interventional Fluoroscopic X-ray System may lose imaging functionality or experience longer restart times. The FDA is recalling approximately 3,011 units of this device worldwide.
Product
Philips Azurion Interventional Fluoroscopic X-ray System with Software Version Number: R1.0, R1.1, R1.2- Intended for Image guidance in diagnostic, interventional, and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2489-2024·2024-08-14
BD PYXIS MEDBANK Automated Cabinet May Print Incorrect Medication Bin Labels
A software issue in the BD PYXIS MEDBANK automated medication dispensing cabinet can cause incorrect bin labels to be printed for restock operations. This could lead to medication administration errors affecting patient safety.
Product
BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P, REF: 169-83 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2509-2024·2024-08-14
Philips IntelliVue Patient Monitors with disabled monitoring software options
Philips IntelliVue Patient Monitors (MX400/450/500/550) with software versions L.x or M.x lack required monitoring capabilities due to removed software entitlements. The missing features could lead to incorrect or delayed patient treatment.
Product
IntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866062. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2514-2024·2024-08-14
Diagnostic Test Kits Recalled for False Vibrio Results With Certain Transport Medium
BioFire Diagnostics is recalling gastrointestinal diagnostic test kits due to false positive Vibrio results when used with certain transport mediums.
Product
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0104 (6 kit test) The BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2539-2024·2024-08-14
Medical Device Hookup Instructions Contain Errors Affecting Endoscope Disinfection
Steris Corporation recalls certain automated endoscope reprocessor hookups due to incorrect instructions in product documentation. Improper hookup connection could prevent proper endoscope disinfection, risking patient infection.
Product
Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated Endoscope Reprocessors ( AER ) and endoscopes, which allow perfusion of liquids dispensed by the AER to contact and high-level disinfect the channels of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2518-2024·2024-08-14
Gyn Laparoscopy Kits Recalled Due to Inadequate Sterilization Process
American Contract Systems is recalling 29 gynecological laparoscopy surgical kits due to insufficient aeration during sterilization, which may compromise sterility and increase infection risk for patients.
Product
American Contract Systems Gyn Laparoscopy convenience kit
Category
Medical Device
Distribution
Distributed nationwide