The Recall Desk

State

Virginia product recalls

72,940 recalls have nationwide distribution and so reach Virginia. 9,479 additional recalls listed Virginia specifically in their distribution scope.

What the numbers show

Total
9,479
Critical
1,285
Severe
2,294
Most recent
2026-09-09

Of the 9,479 recalls naming Virginia we have scored against our rubric, 1,285 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,294 (24%) are Severe.

These figures cover only the 9,479 recalls whose distribution notice names Virginia specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4026–4050 of 82419

  • ModerateFDA (Drugs)·D-0238-2026·2025-12-24

    Cisatracurium 20 mg multiple-dose vials recalled after subpotent assay results

    Somerset Therapeutics is recalling 71,310 vials of Cisatracurium Besylate Injection, 20 mg/10 mL, after out of specification assay results during long term stability testing.

    Product
    CISATRACURIUM BESYLATE — CISATRACURIUM BESYLATE (CISATRACURIUM BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0945-2026·2025-12-24

    Gluteal implants recalled over specification deviations and missing premarket clearance

    DSAART is recalling 118 AART Gluteal Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.

    Product
    Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog Numbers: 501-101 - Gluteal Implant style 1 size 1 UDI-DI code: B490501101 501-103 - Gluteal Implant style 1 size 3 UDI-DI code: B490501103 501-101 UDI-DI code: B490501101 501-103 - Gluteal
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-0937-2026·2025-12-24

    Spinal navigation guide recalled for naming an incompatible toolcard system

    SeaSpine Orthopedics is recalling 310 NorthStar OCT Navigation items because the surgical technique guide incorrectly identified Medtronic Infinity toolcards as compatible.

    Product
    Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012; Navigation Straight Bone Probe, REF: PC2-400013; Navigation, 3.5mm Drill, REF: PC2-400135; Navigation, 4.0mm Drill, REF: PC2-400140; Navigation, 4.5mm Drill, PC2-4001
    Category
    Medical Device
    Distribution
    24 states
  • ModerateFDA (Drugs)·D-0229-2026·2025-12-24

    Lidocaine and epinephrine dental cartridges recalled over cracked containers

    Novocol Pharmaceutical of Canada is recalling 12,033 cartons of Lidocaine HCl 2% with Epinephrine 1:100,000 injection over a defective container with cracked or broken cartridges.

    Product
    LIDOCAINE — LIDOCAINE (LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0237-2026·2025-12-24

    Cisatracurium 200 mg vials recalled after subpotent stability assay results

    Somerset Therapeutics is recalling 28,660 vials of Cisatracurium Besylate Injection, 200mg/20mL, after out of specification assay results during long term stability testing.

    Product
    CISATRACURIUM BESYLATE — CISATRACURIUM BESYLATE (CISATRACURIUM BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0233-2026·2025-12-24

    Carbocaine dental cartridges recalled over cracked and broken containers

    Novocol Pharmaceutical of Canada is recalling 40 cartons of Cook-Waite Carbocaine 3% mepivacaine injection over a defective container with cracked or broken cartridges.

    Product
    CARBOCAINE — CARBOCAINE (MEPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0946-2026·2025-12-24

    Chin implants recalled over specification deviations and missing premarket clearance

    DSAART is recalling 29 AART Chin Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.

    Product
    Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog Numbers: 400-0101 Chin Implant style 1 size 1 UDI-DI code: B490400101 400-0103 Chin Implant style 1 size 3 UDI-DI code: B490400103 400-0104 Chin Implant style 1 size 4 UDI-DI code: B490400104 40
    Category
    Medical Device
    Distribution
    27 states
  • SevereNHTSA·25V906000·2025-12-23

    BMW i4 positive battery cable connection may become loose

    BMW is recalling one 2025 i4 eDrive40 vehicle because the connection between the positive battery cable and the rear power distributor may become loose.

    Product
    BMW — BMW I4 EDRIVE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V907000·2025-12-23

    KTM motorcycle side stand spring may break and fall down

    KTM is recalling certain 2025 390 Adventure R, 390 Adventure X, 390 SMC R and 390 Enduro R motorcycles because engine vibrations may break the side stand spring, letting the stand fall to the ground.

    Product
    KTM — KTM 390 ENDURO R, 390 ADVENTURE X, 390 SMC R, 390 ADVENTURE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V909000·2025-12-23

    Altec Recalls 2022-2023 Aerial Work Platforms Due to Missing Check Valve

    Altec is recalling 2022-2023 AA55, AM55, AN46, and AN55 vehicles because a missing check valve may reduce boom insulation, increasing the risk of electric shock.

    Product
    ALTEC — ALTEC AN46, AM55, AA55, AN55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V911000·2025-12-23

    Honda CBR650R wiring damage can blow the fuse for lights

    Honda is recalling certain 2024-2025 CBR650R motorcycles because engine vibration may damage the turn signal switch wire harness, causing a short circuit and a blown fuse.

    Product
    HONDA — HONDA CBR650R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V908000·2025-12-23

    Volvo rearview camera image may not display when reversing

    Volvo is recalling certain 2021-2025 vehicles across the XC40, XC60, XC90, S60, S90, V60 and V90 ranges because the rearview camera image may not display when the vehicle is in reverse.

    Product
    VOLVO — VOLVO XC90, XC60, V90CC, XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V905000·2025-12-23

    Tiffin motorhome generator wiring harness may contain undersized wires

    Tiffin is recalling certain 2025-2026 Open Trail motorhomes fitted with an optional diesel or propane generator because the wiring harness may contain incorrectly sized wires.

    Product
    TIFFIN — TIFFIN OPEN TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V910000·2025-12-23

    Spartan Fire Emergency Vehicles Recalled for Ladder Handle Defect

    Spartan Fire is recalling certain emergency vehicles because a ladder handle may detach, allowing ground ladders to fall off and creating a road hazard.

    Product
    SPARTAN FIRE — SPARTAN FIRE LEGEND SERIES, STAR SERIES, UST BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V912000·2025-12-23

    2026 Nissan Rogue Vehicles with Incorrect Spare Tire Assembly

    Nissan is recalling 2026 Rogue vehicles with an incorrect-size spare tire that does not match the tire placard information. This may lead to improper tire inflation and increased crash risk.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E092000·2025-12-22

    Couture Co Recalls Specific Volt E-Bike Carriers Due to Latch Wear

    Couture Co is recalling four models of Volt e-bike carriers because the latch mechanism may wear excessively and disengage while driving.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V897000·2025-12-19

    Blue Bird Recalls Electric School Buses Due to Loose 12-Volt Cable

    Blue Bird is recalling 2019-2027 Vision and All American electric school buses because a loose 12-volt cable may disconnect, causing loss of electrical systems.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS (ELECTRIC), ALL AMERICAN SCHOOL BUS (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V898000·2025-12-19

    New Flyer Transit Bus Recall for Antilock Braking System Failure

    New Flyer is recalling certain transit buses because the antilock braking and stability control modules may fail without warning lights, increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XE35, XD35, XE40, XN35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V894000·2025-12-19

    Mercedes-Benz EQB high voltage battery may fail internally and catch fire

    Mercedes-Benz is recalling certain 2022-2023 EQB vehicles because the high voltage battery may fail internally and lead to a vehicle fire while parked or driving.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQB 250, EQB 300 4MATIC, EQB 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·041-2025·2025-12-19

    Olympia Provisions Recalls Holiday Kielbasa Sausage Due to Metal Contamination

    Olympia Provisions is recalling approximately 1,930 pounds of ready-to-eat holiday kielbasa sausages that may contain metal. The recall covers products sold in California, Oregon, and Washington, as well as nationwide online sales.

    Product
    Olympia Provisions — Olympia Provisions Recalls Ready-to-Eat Holiday Kielbasa Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide