The Recall Desk

State

Virginia product recalls

72,992 recalls have nationwide distribution and so reach Virginia. 9,483 additional recalls listed Virginia specifically in their distribution scope.

What the numbers show

Total
9,483
Critical
1,286
Severe
2,296
Most recent
2026-09-25

Of the 9,483 recalls naming Virginia we have scored against our rubric, 1,286 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,296 (24%) are Severe.

These figures cover only the 9,483 recalls whose distribution notice names 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.

6676–6700 of 82475

  • LowFDA (Devices)·Z-1976-2025·2025-06-25

    AcoSound LW12-BTE-M Hearing Aid Labeling and UDI Information Errors

    Hangzhou AcoSound Technology Co., Ltd. is recalling 120 units of the AcoSound Model LW12-BTE-M hearing aid due to labeling errors, including incorrect manufacturer attribution, missing manufacturer business address, and incomplete UDI information.

    Product
    AcoSound. Model Number: LW12-BTE-M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V380000·2025-06-23

    GEM Recalls 2022-2025 Electric Vehicles Due to Ball Joint Separation Risk

    GEM is recalling 2022-2025 e2, e4, e6, and eLXD vehicles because improperly tightened fasteners may cause the front lower ball joint to separate, potentially leading to a loss of steering control.

    Product
    GEM — GEM E6, ELXD, E4, E2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V326000·2025-06-23

    Western Star battery to starter stud can short circuit

    Daimler Trucks is recalling certain 2020-2026 Western Star 49X and 2021-2026 47X vehicles because a stud connecting the battery to the starter at the frame rail may have been incorrectly installed.

    Product
    WESTERN STAR — WESTERN STAR 47X, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V384000·2025-06-23

    Keystone Recalls 2025 Toy Haulers Due to Missing Rear Gate Pins

    Keystone is recalling 2025 Carbon, Fuzion, and Raptor toy haulers because missing rear gate pins or leg support brackets may allow the gate to shift, increasing injury risk.

    Product
    KEYSTONE — KEYSTONE CARBON, RAPTOR, FUZION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V425000·2025-06-20

    Travel trailer patio door transit latch cannot be opened from inside

    Forest River is recalling certain 2025-2026 Wildwood and Salem travel trailers because the exterior transit latch on the rear patio door cannot be unlocked from inside the vehicle.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V423000·2025-06-20

    2026 Forest River Spirit travel trailers recalled for defective safety chains

    Forest River is recalling certain 2026 Spirit travel trailers because the installed safety chains may not meet the actual Gross Vehicle Weight Rating, posing a risk of trailer separation from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER SPIRIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V424000·2025-06-20

    2026 Forest River Sabre Fifth Wheel Griddle Fire Risk Recall

    Forest River is recalling 2026 Sabre fifth wheel recreational trailers because the exterior griddle may be incorrectly installed, allowing it to be stowed while still connected to LPG, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER SABRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V422000·2025-06-19

    Honda Recalls 2013 Accord Vehicles for Driveshaft Corrosion Risk

    Honda is recalling 2013 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because the driveshaft may corrode and break, potentially causing a loss of drive power or vehicle rollaway.

    Product
    HONDA — HONDA ACCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V419000·2025-06-19

    Subaru Forester child seat anchor bolts may come loose

    Subaru is recalling certain 2025 Forester vehicles because the child seat anchor bolts may have been improperly tightened, allowing them to come loose.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V385000·2025-06-19

    Vanguard Recalls 2021-2023 VXP Trailers Due to Hook Box Defect

    Vanguard is recalling 2021-2023 VXP 28-Foot Pup trailers because the pintle hook box assembly may crack or break, reducing stability while being towed.

    Product
    VANGUARD — VANGUARD VXP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V405000·2025-06-19

    Shyft Recalls 2024-2025 Utilimaster Aeromaster for Camera Display Defect

    Shyft Group is recalling 2024-2025 Utilimaster Aeromaster vehicles because the 360-degree camera monitor may not display the correct image at startup, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V421000·2025-06-19

    Supreme Recalls 2025 Wabash Trucks Due to Liftgate Pin Seizure Risk

    Supreme is recalling 2025 Wabash trucks because insufficient lubrication on the liftgate pin may cause it to seize, leading to liftgate failure and injury risk.

    Product
    SUPREME — SUPREME WABASH TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1869-2025·2025-06-18

    Blood Products Administration Set Filter Mis-Assembly Recall

    Fresenius Kabi USA is recalling IVENIX INFUSION SYSTEM LVP Blood Products Administration Sets due to a mis-assembly error that may prevent the drip chamber filter from properly filtering large blood particulates.

    Product
    IVENIX INFUSION SYSTEM LVP Blood Products Administration Set, Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter, 15 mL. Intravascular Administration Set.
    Category
    Medical Device
    Distribution
    18 states
  • SevereFDA (Food)·H-0033-2025·2025-06-18

    Jean's Classy Fresh Salsa Hot recalled due to Salmonella contamination

    TGD Cuts, LLC is recalling Jean's Classy Fresh Salsa, Hot (6/12 oz. plastic tubes) due to Salmonella contamination. The affected product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Jean's Classy Fresh Salsa, Salsa, Hot 6/12 oz., Plastic tube, 6 per case .
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·25V413000·2025-06-18

    Mazda CX-50 airbag module software may cause improper deployment

    Mazda is recalling certain CX-50 Hybrid and CX-50 vehicles because incorrectly configured module software may cause the airbag to deploy improperly. All affected vehicles are under dealer control.

    Product
    MAZDA — MAZDA CX-50 HYBRID, CX-50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25342·2025-06-18

    AstroAI 4-Liter/6-Can Minifridges Recalled Due to Fire and Burn Hazards

    AstroAI is recalling approximately 249,100 minifridges because the electrical switch can short circuit, causing fires and burn hazards. At least 70 incidents of smoking, burning, melting, or fire have been reported, including two fires that caused more than $360,000 in property damage.

    Product
    4 Liter/6 Can Minifridges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0467-2025·2025-06-18

    Male Ultra Pro dietary supplement recalled for undeclared pharmaceutical ingredients

    Male Ultra Pro capsules are being recalled because laboratory testing found undeclared propoxyphenylsildenafil and sildenafil. The product was marketed without an approved New Drug Application.

    Product
    Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1932-2025·2025-06-18

    Philips Intera 1.5T Explorer/Nova Dual MRI Gradient Coil Fire Risk

    Philips is recalling one Intera 1.5T Explorer/Nova Dual MRI system due to a gradient coil component that may overheat, produce smoke, or ignite, risking patient and operator injury.

    Product
    Intera 1.5T Explorer/Nova Dual Product Number: 781108;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1867-2025·2025-06-18

    Z-800W Infusion System Recalled for Unvalidated Software Installation

    Zyno Medical LLC is recalling the Z-800W Infusion System because unreleased software versions were installed on devices without verification or validation.

    Product
    Z-800W Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0037-2025·2025-06-18

    Cucumber Sliced Unpeeled 2 oz. Pack Recalled for Salmonella

    TGD Cuts, LLC is recalling Cucumber Sliced Unpeeled (Item #7065, UPC #840219170657) in 2 oz. packs due to Salmonella contamination. The product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Cucumber Sliced Unpeeled, Pack Size 50, 2 oz. , 50 per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-1866-2025·2025-06-18

    Z-800F Infusion System Recall Due to Unvalidated Software Versions

    Zyno Medical LLC is recalling the Z-800F Infusion System because unreleased software versions were installed on distributed devices without verification or validation. This poses a risk to patients receiving intravenous infusion therapy.

    Product
    Z-800F Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide