State

West Virginia product recalls

72,820 recalls have nationwide distribution and so reach West Virginia. 3,540 additional recalls listed West Virginia specifically in their distribution scope.

What the numbers show

Total: 3,540
Critical: 593
Severe: 656
Most recent: 2026-09-02

Of the 3,540 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 656 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,540 recalls whose distribution notice names West Virginia specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

526–550 of 76360

HighFDA (Devices)·Z-2780-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. DAVINCI PROSTATE PACK DYNJ68477L DYNJ68477M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0709-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled Due to Subpotent Drug Concerns
Major Pharmaceuticals is voluntarily recalling certain lots of Levothyroxine Sodium Tablets (75 mcg) because the medication may be subpotent.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26E050000·2026-07-29
Toyota Recalls Side Curtain Air Bag Assemblies for Tacoma Vehicles
Toyota is recalling side curtain air bag assemblies for 2016-2023 Tacoma vehicles because they may be improperly secured, increasing injury risk during a crash.
Product
AIR BAGS:SIDE/WINDOW:CURTAIN recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0701-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled for Subpotency by Major Pharmaceuticals
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets (50 mcg) from lot N02200 due to subpotency, meaning the tablets may contain less active ingredient than labeled. Products were distributed nationwide in the USA.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2787-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Contamination
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116G
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0711-2026·2026-07-29
LEVOTHYROXINE SODIUM Tablets Recalled Due to Subpotent Drug Content
Major Pharmaceuticals is recalling LEVOTHYROXINE SODIUM 150 mcg tablets because some batches contain less active ingredient than labeled, potentially reducing thyroid hormone effectiveness.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2759-2026·2026-07-29
ICU Medical Recalls Hotline Fluid Warming Sets Due to Leakage Risk
ICU Medical is recalling specific lots of Hotline Fluid Warming Sets due to an increased likelihood of leakage from inadequate solvent application at the tubing to return connector bond.
Product
Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fluids and deliver them to the patient's intravenous access site at normothermic temperatures under gravity flow conditions, List Number L-70
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2793-2026·2026-07-29
SafeOp Patient Interface Neuromonitoring Device Recalled Due to Software Issue
Alphatec Spine, Inc. is recalling the SafeOp Patient Interface due to a software issue that may cause loss of electromyography functionality during surgery.
Product
SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2770-2026·2026-07-29
Penumbra System RED 68 Reperfusion Catheter Recall Due to Fracture Risk
Penumbra, Inc. is recalling its RED 68 Reperfusion Catheter due to manufacturing issues that may cause the device to fracture during use.
Product
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2779-2026·2026-07-29
Medline Bard Silastic Foley Catheter Kits Recalled Due to Surface Contamination
Medline is recalling 980 Bard Silastic Foley Catheter kits due to increased raw material on the catheter surface that may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0726-2026·2026-07-29
Lidocaine Injection Recall Due to Hair Contamination
Fresenius Kabi is recalling lidocaine injection vials after hair was found in the product. The recall affects 181,225 vials distributed nationwide.
Product
LIDOCAINE — LIDOCAINE (LIDOCAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0710-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled Due to Subpotent Drug Concerns
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets (125 mcg) because the medication may be subpotent.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2786-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. SM-LAPAROSCOPIC PROSTATE PAC DYNJ61206J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2794-2026·2026-07-29
Flexible Hystero-Fiberscope Kits Recalled Due to Expired Sterile Seals
Karl Storz Endoscopy is recalling 45 Flexible Hystero-Fiberscope Kits that contain expired Single Use Endoscopic Seals, which could compromise sterility assurance during gynecological procedures.
Product
Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF: 26153EAU/1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2768-2026·2026-07-29
Medtronic Neurosurgery Recalls Ventriculostomy Kit Due to High Endotoxin Levels
Medtronic Neurosurgery is recalling Ventriculostomy Kit (REF: 46154) because endotoxin levels may exceed acceptable limits for devices contacting cerebrospinal fluid.
Product
Ventriculostomy Kit, REF: 46154
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2772-2026·2026-07-29
Halyard STANDARD LINE INSERTION PACK Recall for Silicone Seal Defect
AVID Medical is recalling 112 Halyard STANDARD LINE INSERTION PACKs due to silicone seal defects that may cause fluid leakage or occlusion.
Product
Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2757-2026·2026-07-29
Boston Scientific Steerable Sheath Recall Over Hemostatic Valve Damage
Boston Scientific is recalling its Faradrive Steerable Sheath devices due to potential hemostatic valve damage during preparation, which may cause air ingress and patient harm.
Product
FARADRIVE STEERABLE SHEATH CLEAR OUS, used to facilitate access to the vasculature and into the chambers of the heart, Material Number M004PFCE21M402, IFU Reference Number 51659727-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2755-2026·2026-07-29
FARADRIVE STEERABLE SHEATH CLEAR Medical Device Recall
Boston Scientific recalls FARADRIVE STEERABLE SHEATH CLEAR due to valve damage risk that could cause air embolism during heart procedures.
Product
FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, IFU Reference Number LBL1062
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0727-2026·2026-07-29
Naropin Injection Recall Over Particulate Matter Contamination
Fresenius Kabi is recalling 92,600 vials of NAROPIN (ropivacaine hydrochloride) injection, 0.5%, 10/2028, due to the presence of particulate matter, including hair, found in the product.
Product
NAROPIN — NAROPIN (ROPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2761-2026·2026-07-29
Olympus 4K UHD LCD Monitors Recalled Due to Potential Connector Faults
Olympus Corporation of the Americas is recalling 10 Olympus 4K UHD LCD Monitors (Model OEV321UH) because the HDMI and DisplayPort connectors may become faulty.
Product
Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2675-2026·2026-07-29
BOSS Xe Family Aiming Devices Recalled for Software Safety Enhancement
Wilcox Industries Corp. is recalling BOSS Xe family aiming devices to implement a software enhancement designed to increase safety.
Product
The intended use is to be paired with a weapon for aiming purposes.
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0712-2026·2026-07-29
FDA Recalls Amlodipine and Olmesartan Tablets Over Failed Dissolution Test
Ascend Laboratories is recalling 6,192 bottles of Amlodipine and Olmesartan Medoxomil tablets nationwide due to failed dissolution specifications and Olmesartan content below specifications.
Product
AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2763-2026·2026-07-29
Halyard EYE PACK Convenience Kits Recalled Due to Incorrect Betadine Concentration
AVID Medical, Inc. is recalling certain Halyard EYE PACK convenience kits because the Betadine solution contained within them has an incorrect concentration.
Product
Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0729-2026·2026-07-29
FDA Recalls Xylocaine Injections Due to Hair Contamination
FDA is recalling Xylocaine (lidocaine HCl) injections due to the presence of particulate matter, specifically hair found in the product.
Product
XYLOCAINE — XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2758-2026·2026-07-29
Phantom Hindfoot Guide Rods Recalled Due to Sterile Barrier Breaches
Paragon 28 is recalling specific Phantom Hindfoot TTC/TC Ball Tipped Guide Rods because of complaints regarding breaches in the sterile pouch packaging.
Product
P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped Guide Rod, SIZE: 0.30 mm, LENGTH: 800 mmm, ITem number P31-955-1800-S; provides stabilization of the hindfoot and ankle.
Category
Medical Device
Distribution
Distributed nationwide