The Recall Desk

State

Virginia product recalls

73,218 recalls have nationwide distribution and so reach Virginia. 9,492 additional recalls listed Virginia specifically in their distribution scope.

What the numbers show

Total
9,492
Critical
1,286
Severe
2,302
Most recent
2026-09-25

Of the 9,492 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 2,302 (24%) are Severe.

These figures cover only the 9,492 recalls whose distribution notice names Virginia specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14001–14025 of 82710

  • HighNHTSA·24V062000·2024-02-01

    Tiffin Allegro Bay motorhomes recalled for battery fire risk

    Tiffin is recalling certain 2022–2024 Allegro Bay motorhomes because batteries may shift during travel, causing electrical arcing and fire risk. Dealers will install new hold-down hardware at no charge.

    Product
    TIFFIN — TIFFIN ALLEGRO BAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24105·2024-02-01

    Box Components Recalls BMX Race Bicycle Stems Due to Fall Hazard

    Box Components is recalling about 160 BMX Race Box One Oversized 31.8 Delta bicycle stems because the faceplate can crack and break, loosening handlebars and causing loss of control and crash injury risk. No injuries have been reported to date.

    Product
    BMX Race Box One Bicycle Stems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24099·2024-02-01

    Meijer December Home Light Bulbs Recalled for Burst Hazard

    Meijer is recalling December Home branded candelabra-style light bulbs because some packages contain 3V bulbs instead of the labeled 120V versions. When a 3V bulb is used in a 120V fixture, it can burst, creating a laceration hazard.

    Product
    DECEMBER HOME® Replacement Light Bulbs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24106·2024-02-01

    Glass Little Wanderer Snow Globes Recalled for Laceration Hazard

    The Museum of Modern Art is recalling about 1,915 glass Little Wanderer snow globes sold at MoMA Design Stores because they can crack or fracture, posing a laceration hazard. No injuries have been reported.

    Product
    Snow globes (Little Wanderer)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0781-2024·2024-01-31

    Publix Custom Made Pizzas Recalled Due to Listeria Contamination in Lettuce

    Publix Custom Made Pizzas distributed in eight states are being recalled because the shredded lettuce ingredient may contain Listeria monocytogenes.

    Product
    Publix Custom Made Pizzas, variable weights and sizes, packed in cardboard box, intended for immediate consumption.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0782-2024·2024-01-31

    Publix Custom Burrito Bowls Recalled Due to Listeria Contamination Risk

    Publix Super Markets is recalling Custom Burrito Bowls due to potential Listeria monocytogenes contamination in the shredded lettuce ingredient. The bowls were distributed in Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia during December 5-14, 2023.

    Product
    Publix Custom Burrito Bowls, variable weights and sizes, packed in plastic containers, intended for immediate consumption.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0785-2024·2024-01-31

    Publix Self-Service Salad Recalled for Potential Listeria Contamination

    Publix is recalling self-service salad from its salad bar distributed December 5-14, 2023, in eight states due to potential Listeria monocytogenes contamination in shredded lettuce supplied by Fresh Express.

    Product
    Publix Self Service Salad from the Salad Bar, variable weights and sizes, packed in plastic containers, intended for immediate consumption.
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·24V059000·2024-01-31

    Vicinity Recalls 2017 Vi33 Buses Due to CNG Tank Clearance Issue

    Vicinity is recalling 2017 Vi33 transit buses because inadequate clearance may allow CNG tanks to contact mounting structures, potentially causing damage and gas leaks.

    Product
    VICINITY — VICINITY VI33
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0261-2024·2024-01-31

    Drug recall: Bleomycin injection vials recalled due to glass contamination

    Pfizer is recalling 3,546 vials of Bleomycin for Injection due to the presence of glass particulate matter. The affected lot was distributed nationwide in the USA, Netherlands, and Libya.

    Product
    BLEOMYCIN — BLEOMYCIN (BLEOMYCIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V056000·2024-01-31

    New Flyer Recalls Electric Buses Due to Battery Fire Risk

    New Flyer is recalling 337 electric buses because drain valve issues may allow liquid to accumulate in battery packs, increasing the risk of an electrical short and fire.

    Product
    NEW FLYER — NEW FLYER XE35, XE60, XHE40, XE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V057000·2024-01-31

    Kia EV drive shafts can break under load causing power loss

    Kia is recalling certain 2023-2024 Niro EV and 2023 EV6 vehicles because an improperly heat-treated drive shaft can break under load, resulting in a loss of drive power.

    Product
    KIA — KIA EV6, NIRO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0783-2024·2024-01-31

    Publix Deli Chicken Street Tacos Recalled for Listeria Contamination

    Publix Deli Chicken Street Tacos for Two sold in eight southeastern states are recalled due to potential Listeria monocytogenes contamination in the shredded lettuce ingredient. Consumers should not eat this product and should discard or return it.

    Product
    Publix Deli Chicken Street Tacos for Two, variable weights and sizes, packed in plastic containers, intended for immediate consumption (https://www.publix.com/pd/publix-deli-chicken-street-tacos-for-two/RIO-PCI-238408?origin=search1).
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0784-2024·2024-01-31

    Publix Custom Made Platters Recalled Due to Potential Listeria Contamination

    Publix is recalling custom made platters distributed across eight states due to potential Listeria monocytogenes contamination in the shredded lettuce ingredient. Consumers should not eat platters prepared between December 5-14, 2023.

    Product
    Publix Custom Made Platters, variable weights and sizes, packed in plastic containers, intended for immediate consumption (https://www.publix.com/mc/order-ahead/order-deli-platters?nav=header).
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0317-2024·2024-01-31

    Robitussin Honey CF Max Nighttime Adult Recalled for Microbial Contamination

    Haleon US Holdings LLC is recalling Robitussin Honey CF Max Nighttime Adult cough medicine due to microbial contamination. The FDA Class I recall affects 21,900 bottles distributed nationwide.

    Product
    Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg, Diphenhydramine HCl 25mg), 8 FL OZ (237 mL) bottle, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0316-2024·2024-01-31

    Robitussin Honey CF Max Non-Drowsy Adult recalled for microbial contamination

    GSK Consumer Healthcare recalls Robitussin Honey CF Max Non-Drowsy Adult due to microbial contamination in non-sterile products distributed nationwide. Affected lot numbers carry specific expiration dates.

    Product
    Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg, Dextromethorphan HBr 20 mg), a) 4 FL OZ (118mL) and b) 8 FL OZ (237 mL) bottles, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0780-2024·2024-01-31

    Publix Sub Sandwiches Recalled for Potential Listeria Contamination

    Publix Custom Made Sub Sandwiches are being recalled due to potential Listeria monocytogenes contamination in the shredded lettuce ingredient supplied by Fresh Express. Products were distributed between December 5-14, 2023 in southeastern states.

    Product
    Publix Custom Made Sub Sandwiches, variable weights and sizes, individually wrapped in paper, intended for immediate consumption (https://www.publix.com/menu-subs-and-wraps?merch=hp_viz_nav_subs_wraps).
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0777-2024·2024-01-31

    Outrageous Oat Cookies Recalled for Undeclared Wheat Allergen

    Wegmans Food Markets is recalling Outrageous Oat Cookies due to undeclared wheat. The product poses a serious health risk to consumers with wheat allergies or celiac disease.

    Product
    Outrageous Oat Cookies packaged in 5pk and also sold in Bulk
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·24V058000·2024-01-31

    Heavy truck stability control software has incorrect axle spacing parameters

    Daimler Trucks is recalling certain 2024-2025 Western Star 49X and 2025 Freightliner Cascadia vehicles whose Electronic Stability Control software carries incorrect axle spacing parameters, failing FMVSS 136.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 49X, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0814-2024·2024-01-31

    TactiFlex Ablation Catheter Not Properly Recognized by EnSiteX EP System

    The TactiFlex Ablation Catheter is not correctly recognized by the EnSiteX EP System, which displays it as a different model, prevents certain features from appearing, and may show an inverted image.

    Product
    TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0772-2024·2024-01-31

    VITROS Anti-HBs Immunodiagnostic Products Recalled for Calibration Failures

    Ortho-Clinical Diagnostics is recalling VITROS Immunodiagnostic Products used to test for Hepatitis B antibodies due to potential calibration failures and falsely elevated test results affecting specific lot numbers.

    Product
    VITROS Immunodiagnostic Products Anti-HBs Quantitative Reagent Pack, Catalog No. 6801925 VITROS Immunodiagnostic Products Anti-HBs Calibrators, Catalog No. 6801926
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0786-2024·2024-01-31

    R&B Chocolate Chips Croissant Twist contains undeclared soy lecithin

    Lecoq Cuisine Corporation is recalling R&B Chocolate Chips Croissant Twist because the product contains undeclared soy lecithin. Consumers with soy allergies may be at risk if they consume this product.

    Product
    R&B Chocolate Chips Croissant Twist
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0782-2024·2024-01-31

    Hologic PANTHER FUSION System Recalled for Potential False Positive Flu B Results

    Hologic is recalling PANTHER FUSION nucleic acid testing systems due to the potential for false positive influenza B test results when a sample is also positive for SARS-CoV-2.

    Product
    PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully automates all steps necessary to perform Aptima assays from sample processing through amplification, detection, and data reduction. The Panther Fusion System is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V055000·2024-01-31

    Motorhome retractable awnings can extend unintentionally during transit

    Jayco is recalling certain 2023 Entegra Expanse, Expanse LI, Jayco Solstice and Solstice LI motorhomes because the retractable awning may extend unintentionally while the vehicle is moving.

    Product
    JAYCO — JAYCO, ENTEGRA SOLSTICE, EXPANSE, EXPANSE LI, SOLSTICE LI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0788-2024·2024-01-31

    Power Knee Prosthetic Batteries Recalled Due to Unexpected Shutdown Risk

    Ossur Power Knee prosthetic knee batteries may fail to turn on or shut down unexpectedly, potentially causing users to lose support and fall. Affected units are distributed nationwide.

    Product
    Power Knee, REF: PKA10001, and PKA10003; with Power Knee Battery, REF: PKA10002
    Category
    Medical Device
    Distribution
    Distributed nationwide