State

West Virginia product recalls

73,478 recalls have nationwide distribution and so reach West Virginia. 3,571 additional recalls listed West Virginia specifically in their distribution scope.

What the numbers show

Total: 3,571
Critical: 603
Severe: 872
Most recent: 2026-10-14

Of the 3,571 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 872 (24%) are Severe.

Which agencies issued them

These figures cover only the 3,571 recalls whose distribution notice names West Virginia specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20126–20150 of 77049

HighFDA (Food)·F-1540-2022·2022-08-17
Aivia Whey Protein Chocolate Recalled for Undeclared Milk Allergen
Nature's Sunshine Products is recalling Aivia Whey Protein+ Power Herbs Chocolate because the label declares whey but fails to declare milk. Approximately 2,747 bags were distributed nationwide.
Product
Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904 22711 8 Label is read in parts: "***INGREDIENTS: Whey Isolate, Whey Concentration***".
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1509-2022·2022-08-17
MetaFix hip stem mislabeled with wrong size and batch information
A Corin MetaFix hip stem (size 7 collarless) was incorrectly labeled as a size 3 collared stem with wrong batch information. The labeling error creates risk during surgical implantation.
Product
Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1309-2022·2022-08-17
Lorazepam Injection Recalled for Out-of-Specification Impurities and Degradation
Hikma Pharmaceuticals is recalling Lorazepam Injection vials due to out-of-specification impurities and degradation products found during quality testing of retained samples.
Product
LORAZEPAM — LORAZEPAM (LORAZEPAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1310-2022·2022-08-17
Lorazepam Injection Recalled for Out-of-Specification Impurities and Degradation
Hikma Pharmaceuticals is recalling 82,700 vials of Lorazepam Injection due to failed quality specifications for impurities and degradation. Lot #070096 (expired July 2023) was distributed nationwide.
Product
LORAZEPAM — LORAZEPAM (LORAZEPAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1326-2022·2022-08-17
FDA Recalls Sterile Alcohol Prep Pads Due to Improper Storage
Mckesson Medical-Surgical is recalling ALCOHOL PREP sterile alcohol prep pads nationwide because they were stored outside manufacturer specifications, potentially compromising sterility. FDA classified this as a Class II recall.
Product
ALCOHOL PREP — ALCOHOL PREP (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V631000·2022-08-17
2023 Kenworth and Peterbilt trucks recalled for engine control failure
PACCAR Incorporated is recalling certain 2023 Kenworth and Peterbilt commercial trucks because the engine control module may short-circuit, causing the engine to stall unexpectedly. An engine stall while driving increases the risk of a crash.
Product
PETERBILT — PETERBILT, KENWORTH 520, 579, T680, T800B
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2022·2022-08-17
Xhibit Telemetry Receiver Model 96280 alarm escalation software defect
Xhibit Telemetry Receiver Model 96280 units fail to escalate critical alarms after approximately 25 days of continuous use, including signal loss, low battery, and SpO2 sensor issues. Caregivers may not be aware of device failures.
Product
Xhibit Telemetry Receiver, Model: 96280
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2022·2022-08-17
Lithotripsy Generator Recall Due to Mis-Wired Component Affecting System Reliability
Olympus Corporation recalls 2 units of the ShockPulse-SE Lithotripsy Generator due to a mis-wired component that causes improper power supply noise and EMC non-compliance, potentially affecting device reliability and treatment delivery.
Product
ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1507-2022·2022-08-17
Haiou Needle Retractable Safety Syringe recalls due to needle detachment risk
Approximately 7,218,000 Haiou Needle Retractable Safety Syringes are being recalled due to needle detachment and retracting mechanism failures that increase needlestick injury risk. The affected product was distributed in California.
Product
Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 (0.6x25mm). 200pcs/Box Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-23G25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1313-2022·2022-08-17
Eye Drops Recalled Due to Improper Storage Violating Manufacturing Standards
Naphcon A eye drops are being recalled nationwide because products were stored outside label specifications, violating Current Good Manufacturing Practice (CGMP) standards.
Product
NAPHCON A — NAPHCON A (NAPHAZOLINE HYDROCHLORIDE AND PHENIRAMINE MALEATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1308-2022·2022-08-17
Ativan Lorazepam Injection Recalled Nationwide for Out-of-Specification Impurities
Nationwide recall of Ativan (lorazepam) injection lot 060064Z due to out-of-specification impurities and degradation products. Patients should contact their healthcare provider.
Product
ATIVAN — ATIVAN (LORAZEPAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1319-2022·2022-08-17
FDA Recalls Miralax Osmotic Laxative Powder for Storage Deviations
The FDA recalled 67 bottles of Miralax laxative powder due to storage conditions that violated drug label specifications. The precautionary recall is due to potential product quality concerns from improper storage conditions.
Product
MIRALAX — MIRALAX (POLYETHYLENE GLYCOL 3350)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1306-2022·2022-08-17
Glenmark Pharmaceuticals Recalls Telmisartan/Hydrochlorothiazide Due to Defective Blister Packs
Glenmark Pharmaceuticals Inc., USA is recalling specific lots of Telmisartan and Hydrochlorothiazide tablets due to complaints of defective blister packs that are difficult to open and cause tablets to break during removal.
Product
TELMISARTAN AND HYDROCHLOROTHIAZIDE — TELMISARTAN AND HYDROCHLOROTHIAZIDE (TELMISARTAN AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1329-2022·2022-08-17
Lamotrigine Tablets Recalled for Label Strength Error
AVKARE Inc. is recalling 8,328 bottles of Lamotrigine Tablets, USP 100 mg nationwide due to a labeling error in the declared strength.
Product
LAMOTRIGINE — LAMOTRIGINE (LAMOTRIGINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1314-2022·2022-08-17
FDA Recalls SYSTANE Lubricant Eye Drops Due to Improper Storage
McKesson Medical-Surgical Inc. is recalling 47 bottles of SYSTANE Lubricant Eye Drops nationwide. The products were stored outside label specifications, violating manufacturing practices.
Product
SYSTANE LUBRICANT — SYSTANE LUBRICANT (POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1316-2022·2022-08-17
Eye Drops Recalled for Improper Storage Outside Specifications
SYSTANE BALANCE lubricant eye drops (12 boxes, nationwide) are being recalled because they were stored outside the manufacturer's label specifications. The FDA classified this as a Class II recall.
Product
SYSTANE BALANCE — SYSTANE BALANCE (PROPYLENE GLYCOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1321-2022·2022-08-17
FDA Recalls Pataday Eye Allergy Drops Due to Storage Deviations
Mckesson Medical-Surgical is recalling Pataday Once Daily Relief eye drops nationwide because the products were stored outside label specifications. No illnesses have been reported.
Product
PATADAY ONCE DAILY RELIEF — PATADAY ONCE DAILY RELIEF (OLOPATADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1312-2022·2022-08-17
Bisacodyl suppositories recalled nationwide due to improper storage
McKesson Medical-Surgical is recalling Bisacodyl suppositories stored outside label specifications. The FDA Class II recall affects 45 boxes distributed nationwide.
Product
BISACODYL — BISACODYL (BISACODYL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1327-2022·2022-08-17
Antiseptic Alcohol Swabs Recalled Due to Improper Storage Conditions
McKesson is recalling Dynarex Alcohol Swabsticks nationwide because products were stored outside the conditions specified on the drug label.
Product
ALCOHOL — ALCOHOL (ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1324-2022·2022-08-17
Asthmanefrin Racephinephrine Inhalation Solution Recalled Due to Improper Storage
Asthmanefrin Racephinephrine Inhalation Solution is being recalled because batches were stored outside the conditions specified on the drug label. The recall affects products distributed nationwide.
Product
Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator, For temporary relief of mild symptoms of intermittent asthma, Preservative Free, Sterile, For Oral Inhalation Only, 30 vials per box, Nephron Pharmaceuticals Corporation, NDC 0487-2784-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1305-2022·2022-08-17
Prescription Drug Recall: Telmisartan-Hydrochlorothiazide Tablets Due to Defective Packaging
Glenmark Pharmaceuticals recalls 72,288 units of Telmisartan-Hydrochlorothiazide 80/25 mg tablets nationwide due to defective blister packaging that is difficult to open and causes tablets to break.
Product
TELMISARTAN AND HYDROCHLOROTHIAZIDE — TELMISARTAN AND HYDROCHLOROTHIAZIDE (TELMISARTAN AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1320-2022·2022-08-17
FDA recalls eye ointment for improper storage outside label specifications
GenTeal eye ointment (40 boxes, nationwide) recalled due to CGMP storage deviations. Products were stored outside drug label specifications.
Product
GENTEAL — GENTEAL (MINERAL OIL, WHITE PETROLATUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1323-2022·2022-08-17
FDA Recalls Dakin's Solution Due to Storage Condition Deviations
McKesson Medical-Surgical recalled 113 bottles of Dakin's Solution (sodium hypochlorite) nationwide due to improper storage outside label specifications. Products may have compromised stability.
Product
DAKINS QUARTER — DAKINS QUARTER (SODIUM HYPOCHLORITE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1318-2022·2022-08-17
Earwax Removal Aid Debrox Recalled Nationwide for Improper Storage Conditions
Debrox earwax removal aid is recalled nationwide because 131 boxes of the product were stored outside label-specified conditions. Consumers should discontinue use and consult a healthcare provider if needed.
Product
DEBROX — DEBROX (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1322-2022·2022-08-17
FDA Recalls A&D Original Ointment due to improper storage conditions
A&D Original Ointment 16 oz jars are being recalled nationwide because products were stored outside manufacturer specifications. The recall affects all NDC 11523-0096-3 units distributed in the USA.
Product
A&D Original Ointment, Diaper Rash Ointment & Skin Protectant, 16 oz. Jar, Bayer Healthcare Pharmaceutica, NDC 11523-0096-3.
Category
Drug
Distribution
Distributed nationwide