The Recall Desk

State

Virginia product recalls

73,219 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 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14426–14450 of 82711

  • SevereFDA (Food)·F-0646-2024·2023-12-27

    HMC Farms White Peaches recalled due to potential Listeria contamination

    HMC Farms White Peaches 2lb Gusset Bag are recalled due to potential Listeria monocytogenes contamination. The product was distributed across the United States and internationally.

    Product
    HMC Farms White Peaches 2lb Gusset Bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-0651-2024·2023-12-27

    HMC Farms Peaches Recalled for Potential Listeria Contamination

    HMC Farms Peaches in 4lb boxes are being recalled due to potential contamination with Listeria monocytogenes. The product was distributed to 26 U.S. states and three countries.

    Product
    HMC Farms Peaches 4lb box
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-0652-2024·2023-12-27

    HMC Farms White Nectarines Recalled for Potential Listeria Contamination

    HMC Farms White Nectarines 4lb boxes are being recalled due to potential contamination with Listeria monocytogenes. The product was distributed to 26 U.S. states and internationally.

    Product
    HMC Farms White Nectarines 4lb box
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-0542-2024·2023-12-27

    AirFit F30i Full Face Mask Recalled Due to Magnetic Interference Risk

    ResMed is recalling the AirFit F30i Full Face Mask due to potential magnetic interference with active medical implants and ferromagnetic objects. Safety warnings are being updated.

    Product
    AirFit F30i Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0679-2024·2023-12-27

    Mixed Fruit Luau Bowl recalled for potential Salmonella contamination

    TGD Cuts, LLC is recalling Mix Fruit Luau Bowl products due to potential Salmonella contamination. Affected units were distributed in eight states with use-by dates from November 2-23, 2023.

    Product
    MIX FRUIT LUAU BOWL 3/56 OZ Packaged in clamshell containers. UPC: 840219171753
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0680-2024·2023-12-27

    Mixed Fruit Products Recalled Due to Potential Salmonella Contamination

    TGD Cuts, LLC is recalling Mixed Fruit products in multiple package sizes due to potential Salmonella contamination. The affected products were distributed in nine states.

    Product
    Mixed Fruit: Mixed Fruit 20 lb. UPC: 840219153148. Packaged in buckets Mixed Fruit 5 lb. UPC: 840219116273. Packaged in trays Mixed Fruit 2/5 lb. UPC: 840219153247. Packaged in trays Mixed Fruit 3/40 oz. UPC: 840219175898. Packaged in trays
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0678-2024·2023-12-27

    MIX FRUIT ALOHA BOWL recalled for potential Salmonella contamination

    TGD Cuts, LLC is recalling MIX FRUIT ALOHA BOWL due to potential Salmonella contamination. Affected products were distributed in PA, NJ, MD, WV, SC, VA, DE, NC, and NY.

    Product
    MIX FRUIT ALOHA BOWL 3/48 OZ Packaged in clamshell container. UPC:840219170299
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0647-2024·2023-12-27

    HMC Farms White Nectarines recalled due to potential Listeria contamination

    HMC Farms White Nectarines 2lb Gusset Bags are recalled due to potential contamination with Listeria monocytogenes. The affected product was distributed across the United States and internationally.

    Product
    HMC Farms White Nectarines 2lb Gusset Bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-0648-2024·2023-12-27

    HMC Farms Peaches Recalled Due to Listeria Contamination Risk

    HMC Farms Peaches Signature Farms 2lb bags have been recalled due to potential Listeria monocytogenes contamination. The affected product was distributed widely across the United States and internationally.

    Product
    HMC Farms Peaches Signature Farms 2lb bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-0683-2024·2023-12-27

    Mixed Fruit Cube Recalled for Potential Salmonella Contamination

    TGD Cuts, LLC is recalling Mixed Fruit Cube 1/2" products due to potential Salmonella contamination. The recall affects units distributed in Pennsylvania, New Jersey, Maryland, West Virginia, South Carolina, Virginia, Delaware, North Carolina, and New York.

    Product
    MIXED FRUIT CUBE 1/2"-NO GRA 20 LBS. Packaged in buckets. UPC: 840219191096
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0676-2024·2023-12-27

    Melon Loupe/Dew Chunks Recalled for Potential Salmonella Contamination

    TGD Cuts, LLC is recalling Melon Loupe/Dew Chunks packaged in film due to potential Salmonella contamination. The affected product was distributed in nine northeastern and mid-Atlantic states.

    Product
    MELON LOUPE/DEW CHUNKS 50/2 OZ. Packaged in film. UPC: 840219178080
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-0538-2024·2023-12-27

    AirTouch F20 Full Face Mask Recalled for Magnetic Interference with Medical Implants

    ResMed recalls 3.8 million AirTouch F20 full face masks with magnets that may interfere with active medical implants. Updated safety warnings regarding safe distances from medical devices are being issued.

    Product
    AirTouch F20 Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0650-2024·2023-12-27

    HMC Farms Nectarines Recalled Due to Listeria Contamination Risk

    HMC Farms Nectarines 4lb bags are recalled due to potential Listeria monocytogenes contamination. The recall affects 26 US states, Mexico, Canada, and Taiwan.

    Product
    HMC Farms Nectarines 4lb bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-0515-2024·2023-12-27

    Sterile Water Syringes recalled for lack of sterility assurance

    Nurse Assist LLC recalls sterile water injection and irrigation syringes for inadequate sterility assurance. Affected products may be nonsterile and could cause infection if used.

    Product
    Sterile Water: Product Name/Product Code: USP STERILE WATER SYRINGE/1030A, SYRINGE PREFILLED 10 ML/6496722, 30CC PREFILLED SYRINGE/6496723, USP STERILE WATER SYRINGE/1030, 10CC PREFILLED SYRINGES/51638, 30CC PREFILLED SYRINGES/52333, 10CC PREFILLED SYRINGES/1010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0675-2024·2023-12-27

    Fruit Tray with Dip Recalled Due to Potential Salmonella Contamination

    TGD Cuts, LLC is recalling fruit trays with dip due to potential Salmonella contamination. The affected products were distributed across nine states in the Northeast and Mid-Atlantic regions.

    Product
    FRUIT TRAY W/DIP 3/5 LB, 3/36 OZ, 3/56 OZ, and 3/40OZ UPCs: 840219175454, 840219195926, and 840219171777. Packaged in trays.
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-0539-2024·2023-12-27

    AirFit N20 Nasal Mask: Magnetic Interference with Medical Implants

    ResMed AirFit N20 Nasal Masks contain magnets that may interfere with active medical implants and ferromagnetic objects. The FDA classified this as Class I; ResMed is updating safety warnings with required distances.

    Product
    AirFit N20 Nasal Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0608-2024·2023-12-27

    RAPIDPoint 500 Measurement Cartridge Sodium Sensor May Cause Measurement Error

    Siemens RAPIDPoint 500 cartridges may produce inaccurate sodium measurements in blood samples, potentially delaying diagnosis or causing inappropriate treatment. The sodium sensor may show a negative bias, affecting patient care.

    Product
    RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10491448
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0589-2024·2023-12-27

    Acrobat-i Vacuum Positioner System Recalled for Positioner Arm Locking Failure

    Maquet Cardiovascular is recalling the Acrobat-i Vacuum Positioner System because the positioner arm may fail to tighten or lock during normal use, which could affect surgical positioning.

    Product
    Acrobat-i Vacuum Positioner System, Model Number XP-5000Z
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0609-2024·2023-12-27

    RAPIDPoint 500 Measurement Cartridge Sodium Sensor Negative Bias Risk

    Siemens RAPIDPoint 500 measurement cartridges may produce inaccurate sodium readings, risking delayed diagnosis of dangerous electrolyte imbalances or unnecessary treatment.

    Product
    RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10491449
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0559-2024·2023-12-27

    Philips Azurion Ceiling-Mount Systems Rotation Cover May Fall

    Philips is recalling Azurion ceiling-mount imaging systems because a rotation cover may fall if the L-arm collides with hospital equipment, potentially causing injury or affecting sterilization.

    Product
    Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion 7 M12 722079 Azurion 7 M20 722223 Azurion 7 M12 722224 Azurion 7 M20 722227 Azurion 5 M12 722228 Azurion 5 M20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0579-2024·2023-12-27

    Exactech Equinoxe Shoulder System recalled for vacuum loss in bags

    Exactech Equinoxe Reverse Shoulder implants have been recalled due to loss of vacuum in the storage bag. The manufacturer received 3 complaints involving 4 devices.

    Product
    Exactech Equinoxe Reverse Shoulder System, Catalog Numbers: a) 320-36-00, b) 320-36-03, c) 320-36-04, d) 320-36-10, e) 320-36-13, f) 320-38-00, g) 320-38-13, h) 320-40-00, i) 320-40-10, j) 320-42-00, k) 320-42-10, l) 320-42-13, m) 320-46-10, n)…
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0567-2024·2023-12-27

    AC Power Adapter for LIFEPAK 15 Defibrillator May Fail to Charge or Power On

    AC power adapters for LIFEPAK 15 Monitor/Defibrillators may fail to charge batteries or power on the device. Physio-Control is recalling 18,732 units manufactured between November 2021 and April 2023.

    Product
    AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0581-2024·2023-12-27

    Exactech Novation Hip System Recalled for Vacuum Seal Loss

    Exactech is recalling the Novation Hip System due to loss of vacuum in the sterile packaging. The company has received complaints about this defect affecting 4 devices.

    Product
    Exactech Novation Hip System, Catalog Numbers: 134-36-45
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0585-2024·2023-12-27

    Exactech Truliant Knee System Recalled Due to Vacuum Bag Failure

    Exactech recalls certain Truliant Knee System units due to loss of vacuum in the inner vacuum bag. The affected units were distributed across multiple U.S. states and international locations.

    Product
    Exactech Truliant Knee System, Catalog Numbers: a) 02-012-35-3509, b) 02-022-35-1509, c) 02-022-35-1513, d) 02-022-35-3010, e) 02-022-35-3509, f) 02-022-35-3510, g) 02-022-35-3511, h) 02-022-35-4511, i) 02-022-44-3512, j) 02-022-47-2509, k) 02-022-51-4519
    Category
    Medical Device
    Distribution
    16 states