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.

6701–6725 of 82475

  • SevereFDA (Food)·H-0032-2025·2025-06-18

    Jean's Classy Fresh Salsa Mild recalled for Salmonella contamination

    TGD Cuts, LLC is recalling Jean's Classy Fresh Salsa, Mild (12 oz. glass jars) due to Salmonella contamination. The product was distributed in Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Jean's Classy Fresh Salsa, Mild, 12 oz. Glass Jars, 6 per case.
    Category
    Food
    Distribution
    5 states
  • 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
  • SevereCPSC·25351·2025-06-18

    MaxKare Electric Blankets Recalled for Burn and Fire Hazards

    MaxKare electric blankets (model HB18A) sold on Walmart.com can overheat and catch fire, posing burn hazards. Yumo has received 34 reports of overheating, including 3 burn injuries and 2 fires.

    Product
    MaxKare Electric Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1952-2025·2025-06-18

    Tecfen Medical 2.8mm Slit Knife Angled Sterility Assurance Recall

    Tecfen Medical is recalling 2.8mm Slit Knife, Angled (Model QKN2808) ophthalmic surgical instruments due to sterility assurance concerns. Affected units were distributed in the US and internationally.

    Product
    Brand Name: Tecfen Medical Product Name: 2.8mm Slit Knife, Angled Model/Catalog Number: QKN2808 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile (gamma radiation) and packaged individually in Tyvek 1059B. Slit knive
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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
  • 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 (Devices)·Z-1972-2025·2025-06-18

    BD Texium Closed System Drug Transfer Devices May Leak at Connector

    BD Texium closed system drug transfer devices in multiple sizes may leak at the interface between the male luer component and needle-free connector, potentially causing treatment delays, exposure to hazardous drugs, and underdosing.

    Product
    BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: MY8020-0006; 30 mL, REF: MY8030-0006; 60 mL, REF: MY8060-0006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0464-2025·2025-06-18

    MALEXTRA Dietary Supplement Recalled for Undeclared Pharmaceutical Ingredients

    MALEXTRA Recharge with Extra dietary supplement is being recalled nationwide because laboratory testing found undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil in the product.

    Product
    MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, UPC B0CWKZ6ZP3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0030-2025·2025-06-18

    Cucumber Super Selec from Lipman Produce Recalled for Salmonella Risk

    Lipman Family Farms is recalling Cucumber Super Selec products due to potential Salmonella contamination. The affected cucumbers were distributed across multiple states.

    Product
    Cucumber Super Selec Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Devices)·Z-1963-2025·2025-06-18

    Microtek Patient Drape Adapter Plug Kits Recalled for Non-Sterile Labeling

    Microtek Medical is recalling Patient Drape adapter plug kits (models AP6MMN and AP8MMN) because non-sterile products were labeled as sterile. The affected adapters are used to connect drain hoses to fluid management devices.

    Product
    Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN Patient Drape, 8mm Adapter Plug Kit REF AP8MMN UDI code: (01)10748426139429 These adapters function as accessories for a device or drape, serving to
    Category
    Medical Device
    Distribution
    20 states
  • SevereFDA (Devices)·Z-1928-2025·2025-06-18

    Philips Achieva XR MRI systems recall for fire hazard

    Philips Achieva XR MRI systems may have a gradient coil component failure that can generate heat, smoke, and fire. The risk to patients and operators includes inhalation of smoke, burns, and asphyxia.

    Product
    Achieva XR Product Numbers: (1) 781153, (2) 781253;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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
  • 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-1915-2025·2025-06-18

    Covidien Newport HT70 and HT70Plus Ventilators Capacitor Failure Recall

    Covidien is recalling Newport HT70 and HT70Plus ventilators due to capacitor failures that may cause the device to shut down unexpectedly or fail to alarm, risking respiratory failure and oxygen deprivation in patients.

    Product
    Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU, HT70M-WW-NA, HT70-SY-EU. Newport HT70Plus Ventilator, REF: HT70PM-ES-EU, HT70PM-ES-NA, HT70PM-JP-NA, HT70PM-PT-BR, HT70PM-SY-AS, DLHT70PM-WW-NA, HT70PM-SY-NA, HT70PM-SY-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0463-2025·2025-06-18

    Dietary Supplement Male Ultra Recalled for Undeclared Drug Ingredients

    Male Ultra dietary supplement, distributed nationwide in 3,000 boxes, has been recalled because laboratory testing found it contains undeclared pharmaceutical ingredients: propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.

    Product
    Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1936-2025·2025-06-18

    Philips SmartPath to dStream 1.5T MRI Gradient Coil Fire Risk

    Philips SmartPath to dStream for 1.5T MRI systems are recalled due to potential gradient coil component failure that may produce smoke and fire, posing risks of inhalation injury, burns, asphyxia, and death.

    Product
    SmartPath to dStream for 1.5T¿; Product Number: 782146;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1931-2025·2025-06-18

    Philips Intera 1.5T Achieva Nova-Dual MRI System Fire Hazard Recall

    Philips is recalling three Intera 1.5T Achieva Nova-Dual MRI systems worldwide due to a gradient coil component failure that can generate smoke and fire, posing risks including burn injury and asphyxia.

    Product
    Intera 1.5T Achieva Nova-Dual Product Number: 781173;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·25345·2025-06-18

    TADAKAZU Baby Loungers Recalled for Suffocation Fall and Entrapment Hazards

    TADAKAZU Baby Loungers violate federal infant sleep product standards, posing risks of suffocation, falls, and entrapment. The CPSC recommends immediate discontinuation and contact with TADAKAZU for refund.

    Product
    TADAKAZU Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1921-2025·2025-06-18

    SOLTIVE Premium SuperPulsed Laser System surgical instrument thermal incident

    Olympus is recalling the SOLTIVE Premium SuperPulsed Laser System due to risk of thermal incidents including smoke, sparks, burning, or flames during clinical use caused by fiber fracturing.

    Product
    Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed Laser System Model/Catalog Number: TFL-PLS, TFL-PLS-JA (Japan only); Software Version: N/A Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0026-2025·2025-06-18

    Cucumbers Recalled Due to Potential Salmonella Contamination

    Lipman Family Farms is recalling 24-count repacked cucumbers distributed across 18 states due to potential Salmonella contamination. Consumers should not consume the product and should discard or return affected cucumbers.

    Product
    Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·H-0039-2025·2025-06-18

    Cucumber and Grape Tomato Product Recalled for Salmonella Contamination

    TGD Cuts, LLC is recalling Cucumber Sliced/Grape Tomato 50/2oz. packs due to Salmonella contamination. The affected product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Cucumber Sliced/Grape Tomato 50/2oz. Pack, 50 per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-1929-2025·2025-06-18

    Philips Intera 1.5T Achieva IT Nova MRI System Gradient Coil Fire Risk

    Philips is recalling one Intera 1.5T Achieva IT Nova MRI system due to a gradient coil component that may overheat and produce smoke or fire, posing risks of inhalation injury, burns, or death.

    Product
    Intera 1.5T Achieva IT Nova Product Number: 781175
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0023-2025·2025-06-18

    East Coast Fresh Salsa Products Recalled for Potential Salmonella Contamination

    Sysco Corporation is recalling multiple East Coast Fresh salsa products distributed across 18 states and Puerto Rico due to potential Salmonella contamination in cucumbers used in the product.

    Product
    RTSALSA1LB 1# EAST COAST FRESH Salsa Cup - 1 lb ALL LOT CODES SAL20 5# EAST COAST FRESH EC-Salsa- Fresh 5# ALL LOT CODES SAL210 6/1# EAST COAST FRESH Salsa- Fresh Retail 6x1# (E) ALL LOT CODES SAL45 20# EAST COAST FRESH EC-Salsa- Fresh 20# ALL LOT CODES SAL48 7# EAST COAST FRESH
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·H-0035-2025·2025-06-18

    Jean's Classy Fresh Salsa Recalled Due to Salmonella Contamination

    Jean's Classy Fresh Salsa, Mild (5 lbs.) is being recalled due to Salmonella contamination. The product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Jean's Classy Fresh Salsa, Salsa, Mild 5 lbs. 1 per case .
    Category
    Food
    Distribution
    5 states