State

West Virginia product recalls

73,092 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 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8976–9000 of 76662

SevereFDA (Devices)·Z-0296-2025·2024-11-20
Philips LifeVent EVO2 ventilators recalled for potential sensor accuracy failure
Philips Respironics is recalling LifeVent EVO2 ventilators due to potential aerosol deposit accumulation on the internal flow sensor that could cause inaccurate measurements during ventilation.
Product
LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0290-2025·2024-11-20
Trilogy Evo O2 Ventilators Recalled for Potential Flow Sensor Malfunction
Philips Respironics recalled 24,249 Trilogy Evo O2 ventilators because in-line nebulizer configurations may allow aerosol deposits to accumulate on the device's flow sensor, potentially causing inaccurate flow measurements.
Product
Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B, EE2100X15B, FX2100X15B, ES2100X15B, ND2100X15B, FR2100X14B, IT2100X21B, JP2100X16B, IN2100X19, EU2100X19. Intended for invasive and non-invasive ventilation of pedi
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0292-2025·2024-11-20
Trilogy Evo Universal Ventilator Recalled Due to Sensor Malfunction Risk
Trilogy Evo Universal Ventilators (Model DS2000X11B) are recalled because in-line nebulizer configuration in certain locations could cause aerosol accumulation on the internal flow sensor, potentially resulting in inaccurate measurements.
Product
Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V877000·2024-11-20
Hyundai Tucson console wiring may allow shifting out of Park unbraked
Hyundai is recalling certain 2025 Tucson and Santa Cruz vehicles because misrouted console wiring may allow the transmission to shift out of Park without the brake applied.
Product
HYUNDAI — HYUNDAI SANTA CRUZ, TUCSON
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0295-2025·2024-11-20
Ventilator Model LD2110X23B Recalled for Potential Sensor Measurement Failure
Philips Respironics is recalling 1,322 Garbin Evo ventilators (Model LD2110X23B) worldwide due to potential aerosol accumulation that could cause inaccurate flow sensor readings, posing a risk to patient care.
Product
Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0291-2025·2024-11-20
Philips Trilogy Evo ventilators recall: flow sensor fouling risk
Philips Respironics is recalling Trilogy Evo ventilators due to potential aerosol deposits on the internal flow sensor, which could cause inaccurate flow measurements during ventilation.
Product
Trilogy Evo. Model Numbers: DS2110X11B, UDS2110X11B, RDS2110X11B, CA2110X12B, JP2110X16B, IN2110X15B, DE2110X13B, AU2110X15B, BL2110X15B, EU2110X15B, BR2110X18B, LA2110X15B, EE2110X15B, FR2110X14B, GB2110X15B, ND2110X15B, ES2110X15B, IA2110X15B, IT2110X21B, KR2110X15B, TR2110X15B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0406-2025·2024-11-20
AVID Medical Recalls Halyard C Section Bundles Due to Metal Flakes
AVID Medical, Inc. is recalling Halyard C Section Bundles because small metal flakes may detach from sponge forceps and towel clamps, posing a risk of foreign body reactions.
Product
Halyard C SECTION BUNDLE - Medical convenience kits Model Number: LANC015-34
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0404-2025·2024-11-20
AVID Medical Recalls Halyard Laparoscopy Trays Due to Metal Flakes
AVID Medical is recalling 42 Halyard Laparoscopy Trays because sponge forceps and towel clamps may release metal flakes that could enter a patient's surgical site.
Product
Halyard LAPAROSCOPY TRAY - Medical convenience kits Model Number: LANC006-25
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0357-2025·2024-11-20
Medline Recalls Non-Sterile Urinalysis Kit Specimen Containers
Medline Industries is recalling 626,305 urinalysis kits because the specimen containers are labeled sterile but are non-sterile, posing a risk of unnecessary treatment or hospitalization.
Product
URINALYSIS KIT 4, SKU DYLAB1021; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24E099000·2024-11-20
Agility Fuel Solutions Recalls CNG Fuel Systems Due to Valve Cracks
Agility Fuel Solutions is recalling certain CNG fuel systems because manual cylinder valves may develop stress corrosion cracks, causing a natural gas leak that increases fire risk.
Product
FUEL SYSTEM, OTHER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24E098000·2024-11-20
Lippert Recalls Fifth Wheel Pin Boxes Due to Fastener Issues
Lippert is recalling specific Curt Helux Pin Boxes installed in Lippert 5W Chassis because fasteners may be improperly tightened, increasing crash risk.
Product
TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0293-2025·2024-11-20
Trilogy EV300 ventilator: potential flow sensor malfunction from aerosol accumulation
Philips Respironics is recalling 34,146 Trilogy EV300 ventilators due to potential aerosol accumulation on the internal flow sensor, which could cause inaccurate ventilation measurements.
Product
Trilogy EV300. Model Numbers: DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B, GB2200X15B, ND2200X15B, ES2200X15B, FR2200X14B, FX2200X15B, EU2200X15B, IA2200X15B, IT2200X21B, KR2200X15B, TR2200X15B, EE2200X15B. Intended for invasive and non-invasive venti
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0383-2025·2024-11-20
Medical Drainage Pack Components Recalled for Potential Metal Fragments
AVID Medical is recalling the Halyard IR Abcess Drainage Pack due to sponge forceps and towel clamps that may have loose metal flakes. Metal flakes could detach and enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard IR ABCESS DRAINAGE PACK - Medical convenience kits Model Number: AVMD018
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0410-2025·2024-11-20
Halyard Knee Arthroscopy Packs recalled due to loose metal flakes
AVID Medical recalls Halyard Knee Arthroscopy Packs due to loose metal flakes that could detach from forceps and clamps. Metal fragments may enter the surgical site, potentially causing local or foreign body reactions.
Product
Halyard KNEE ARTHROSCOPY PACK - Medical convenience kits Model Number: MAMC204-16
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0360-2025·2024-11-20
Urine kit specimen containers recalled for non-sterile condition
Medline urine kit specimen containers labeled as sterile are actually non-sterile. This risks sample contamination, infection, and unnecessary treatment.
Product
URINE KIT, SKU DYKM1845; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0366-2025·2024-11-20
Stryker electrosurgical smoke evacuation pencils recalled for unintended activation risk
Stryker is recalling smoke evacuation pencils used in electrosurgery that may activate without manual input, creating a risk of electrical burns to patients or healthcare providers.
Product
Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch, Bulk Non-Sterile - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuat
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0355-2025·2024-11-20
Medical Laboratory Kit Recalled Due to Non-Sterile Specimen Container
Medline Industries is recalling over 626,000 laboratory kits because the included specimen container is labeled as sterile but is actually non-sterile. Non-sterile containers risk sample contamination and may result in unnecessary treatment or prolonged hospitalization.
Product
Lab Kit, SKU DYLAB1018; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0384-2025·2024-11-20
Halyard IR Biopsy Pack recalled for loose metal flakes in surgical kit
AVID Medical is recalling Halyard IR BIOPSY PACK due to loose metal flakes in forceps and towel clamps that could detach and enter the surgical site, potentially causing local or foreign body reactions.
Product
Halyard IR BIOPSY PACK - Medical convenience kits Model Number: AVMD019-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0430-2025·2024-11-20
Halyard SAMMC ANGIOGRAPHY Medical Kits Recalled for Loose Metal Flakes
AVID Medical recalls Halyard SAMMC ANGIOGRAPHY medical convenience kits due to loose metal flakes on sponge forceps and towel clamps. Metal flakes may enter surgical sites, potentially causing local reactions or foreign body complications.
Product
Halyard SAMMC ANGIOGRAPHY - Medical convenience kits Model Number: SAMM066-15
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0414-2025·2024-11-20
Halyard Surgical Kit Components May Shed Metal Flakes
AVID Medical is recalling Halyard ANGIO ARTERIOGRAM PACK surgical kits due to metal flakes that may detach from forceps and clamps. Metal fragments could enter a patient's surgical site and cause local or foreign body reactions.
Product
Halyard ANGIO ARTERIOGRAM PACK - Medical convenience kits Model Number: MMCC004-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0440-2025·2024-11-20
Halyard Biopsy Pack surgical instruments recalled due to loose metal flakes
AVID Medical is recalling Halyard BIOPSY PACK surgical kits due to loose metal flakes from sponge forceps and towel clamps. Metal flakes could enter a patient's surgical site, potentially causing local or foreign body reactions.
Product
Halyard BIOPSY PACK - Medical convenience kits Model Number: VANW019-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0356-2025·2024-11-20
UA Kit Specimen Containers Identified as Non-Sterile Despite Sterile Labeling
MEDLINE's UA Kit specimen containers are labeled as sterile but have been identified as non-sterile, posing a risk of contaminated specimens that could lead to incorrect test results and unnecessary treatment.
Product
UA KIT, SKU DYKM1690A; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2025·2024-11-20
MEERA CL Mobile Operating Table Control Malfunction Recall
The MEERA CL mobile operating table may experience error code 50037 that stops table movement during use, causing surgical procedure delays. Getinge recalled 342 units distributed worldwide.
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment, Item Number: 720001B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0329-2025·2024-11-20
SafeControl Bed Handset May Move Unexpectedly After Power Restoration
The SafeControl handset component of Sentida beds may revert to an active mode after power restoration, potentially causing unintended bed movement. Consumers should ensure beds are safely positioned before power interruptions.
Product
SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers: 01-011539, 01-011541, 01-01198
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0454-2025·2024-11-20
Medical convenience kits recalled due to detachable metal flakes
AVID Medical is recalling Halyard PACEMAKER PK medical convenience kits because sponge forceps and towel clamps may shed loose metal flakes that could enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard PACEMAKER PK - Medical convenience kits Model Number: WKMC120-02
Category
Medical Device
Distribution
Distributed nationwide