The Recall Desk

State

Virginia product recalls

20,187 recalls have nationwide distribution and so reach Virginia. 0 additional recalls listed Virginia specifically in their distribution scope.

About recalls in Virginia

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Virginia consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

7676–7700 of 20187

  • HighCPSC·24363·2024-09-12

    Bright Builder Fort Kits recalled for button cell battery ingestion hazard

    Intellio Toys is recalling Bright Builder fort kits because the included flashlights have button cell batteries in compartments that open easily without tools. Swallowed button cell batteries can cause serious internal injuries, chemical burns, and death.

    Product
    Bright Builder Fort Kits with Flashlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V871000·2024-09-12

    2023 Land Rover Range Rover Sport Exterior Lights May Fail

    Moisture may accumulate in the right-side tailgate and lights of certain 2023 Land Rover Range Rover Sport vehicles, causing exterior lights to fail and reducing visibility.

    Product
    LAND ROVER — 2023 LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V881000·2024-09-12

    2022-2023 Mercedes-Benz Metris Fuel Pump May Fail Unexpectedly

    The fuel pumps in certain 2022-2023 Mercedes-Benz Metris vehicles may shut down unexpectedly, causing loss of drive power and increasing the risk of a crash.

    Product
    MERCEDES-BENZ — 2022 MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V882000·2024-09-12

    2024 Nissan Altima Recall for Potential Steering Bolt Loosening

    Nissan is recalling approximately 5 certain 2024 Altima vehicles because bolts connecting the electronic power steering unit to the steering rack may loosen, potentially causing loss of steering control or lock-up. Dealers will replace the steering gear assembly at no cost.

    Product
    NISSAN — 2024 NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V869000·2024-09-12

    2024 Chevrolet Equinox door strikers may fracture and open unexpectedly

    General Motors is recalling certain 2024 Chevrolet Equinox and related models because door strikers may fracture, potentially causing doors to open unexpectedly while driving.

    Product
    CHEVROLET — 2024 CHEVROLET EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V915000·2024-09-12

    Kenworth and Peterbilt Trucks Recalled for Faulty Electronic Control Units

    PACCAR is recalling 2021-2025 Kenworth and Peterbilt commercial trucks with defective electronic control units that may fail due to electrical interference, potentially disabling critical safety systems including ABS, traction control, and electronic stability control.

    Product
    KENWORTH — 2021 KENWORTH W900B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24357·2024-09-12

    Stanley Jr. Kids Garden Sets Recalled for Excessive Lead in Paint

    Red Toolbox is recalling Stanley Jr. Kids Wheelbarrow and 7-piece Garden Sets sold at Costco because the painted long hoe and rake contain lead levels exceeding the federal ban, creating a poisoning hazard for children.

    Product
    Stanley Jr. Kids Wheelbarrow and 7-piece Garden Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V880000·2024-09-12

    Mercedes-Benz vehicles recalled for fuel pump failure affecting drive power

    Mercedes-Benz is recalling 2021–2024 vehicles due to fuel pump failures that may cause loss of drive power, increasing crash risk. Dealers will provide free replacement.

    Product
    MERCEDES-BENZ — 2023 MERCEDES-BENZ AMG E63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V876000·2024-09-12

    Mercedes-Benz and Freightliner Sprinter Partition Wall Recall for Missing Bolts

    Daimler Vans USA is recalling 2019-2023 Mercedes-Benz and 2019-2021 Freightliner Sprinter vehicles whose partition walls may have missing bolts. The loose wall could detach during a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — 2020 MERCEDES-BENZ SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24361·2024-09-12

    GOETAS Pool Drain Covers Recalled for Entrapment Hazard

    GOETAS pool drain covers do not meet Virginia Graeme Baker Pool and Spa Safety Act requirements and pose an entrapment hazard to swimmers. About 2,500 units sold on Amazon.com from March 2022 through July 2024 are affected.

    Product
    GOETAS Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24362·2024-09-12

    MJKSARE High Chairs Recalled for Entrapment and Fall Hazards

    MJKSARE high chairs are recalled due to excessively wide leg openings that pose an entrapment hazard to infants and a fall hazard from a disengageable tray. About 4,760 units sold on Amazon from February to March 2024 are affected.

    Product
    MJKSARE High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2943-2024·2024-09-11

    Trilogy Evo Ventilator Software Update for Identified Safety Issues

    Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for the Trilogy Evo Universal Ventilator to address safety issues identified in earlier recalls. Affected units should implement the update.

    Product
    Trilogy Evo Universal Ventilator, Model No. DS2000X11B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2942-2024·2024-09-11

    Trilogy Evo EV300 Ventilator Mandatory Software Update for Safety Issues

    Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo EV300 ventilators to resolve previously identified safety issues. Approximately 90,910 US units and 56,273 international units are affected.

    Product
    Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benelux EV300; BR2200X18B Trilogy Evo, O2, Brazil EV300; CA2200X12B Trilogy Evo, O2, Canada EV300; DE2200X13B Trilogy Evo, O2, Germany EV300; DS2200X11B Trilogy Evo, O2, USA EV300; DS2200X11B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0649-2024·2024-09-11

    FDA Recalls Heparin Sodium Injection for Endotoxin Contamination

    Baxter Healthcare Corporation is recalling 44,208 containers of Heparin Sodium in Sodium Chloride Injection nationwide after endotoxin testing revealed out-of-limit results. The contamination poses a risk of serious adverse reactions in patients receiving the intravenous medication.

    Product
    HEPARIN SODIUM IN SODIUM CHLORIDE — HEPARIN SODIUM IN SODIUM CHLORIDE (HEPARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2944-2024·2024-09-11

    Philips Respironics Trilogy Evo Ventilator Software Update Addresses Safety Issues

    Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo ventilators worldwide to resolve identified safety issues. Users must apply the update and review the updated User Manual.

    Product
    Trilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL2110X15B Trilogy Evo, Benelux BR2110X18B Trilogy Evo, Brazil CA2110X12B Trilogy Evo, Canada DE2100X13B Trilogy Evo O2, Germany DE2110X13B Trilogy Evo, Germany DS2100X11B Trilogy Evo, O2, US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2690-2024·2024-09-11

    Vivo 45 LS Ventilator Recall: Potential Formaldehyde Emission Risk

    Breas Medical is recalling the Vivo 45 LS ventilator due to potential elevated formaldehyde emissions into the patient breathing airpath under specific conditions.

    Product
    Vivo 45 LS, pressure and volume ventilator capable of delivering continuous or intermittent ventilatory support for patients who require invasive or non-invasive mechanical ventilation, Model/Catalog Number: 230000 (230016, 230216)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1781-2024·2024-09-11

    Popsicle Jolly Rancher Frozen Pops Recalled for Undeclared Milk Allergen

    Unilever North America is recalling Popsicle Jolly Rancher Frozen Confection Pops nationwide due to undeclared milk, which poses a risk to consumers with milk allergies.

    Product
    Popsicle Jolly Rancher Frozen Confection Pop Net Wt 2.71 FL OZ (80 ML). Green Apple Blue Raspberry and Grape flavored. GTIN/UPC 10077567003727 Case UPC 77567003720
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V782000·2024-09-11

    2023 Honda HR-V Seat Belt Pretensioner Assembly May Fail to Restrain

    Honda is recalling certain 2023-2024 HR-V vehicles because the front seat belt pretensioners may be missing a rivet, which could cause the restraint to fail during a crash.

    Product
    HONDA — 2023 HONDA HR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2966-2024·2024-09-11

    Impella 5.5 Pump Labeling Updated Due to Device Interaction

    Abiomed updated Impella 5.5 cardiac pump labeling to document a potential interaction with Shockwave Coronary IVL Catheter during coronary procedures. No injuries have been reported.

    Product
    Impella 5.5 SmartAssist Set, JP; Product Code: 1000211;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2948-2024·2024-09-11

    BD Pyxis QFill Medication Cabinet Software Bug Causes Incorrect Restock Labels

    The BD Pyxis QFill Replenishment Station medication cabinet has a software issue that may print incorrect bin information on restock labels for medications stored in non-CUBIE locations.

    Product
    BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2970-2024·2024-09-11

    Impella 5.5 SmartAssist S2 Labeling Updated for Shockwave Catheter Interaction

    Abiomed is updating labeling for the Impella 5.5 SmartAssist S2 cardiac assist device to address a potential interaction with Shockwave Coronary IVL Catheters during coronary interventions.

    Product
    Impella 5.5 SmartAssist S2 Set, JP; Product Code: 1000459;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2024·2024-09-11

    Beckman Coulter DxI 9000 Analyzer Recalled for Leaking Wash Buffer Tank

    Beckman Coulter is recalling 17 DxI 9000 Access Immunoassay Analyzers due to cracks in the Internal Wash Buffer Tank that can cause leaking, potentially delaying test results and exposing users to chemical and physical hazards.

    Product
    DxI 9000 Access Immunoassay Analyzer, REF C11137, vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2979-2024·2024-09-11

    Power Express PE Centrifuge adhesive joint failure may cause component detachment

    The adhesive joint in this medical device component can fail, causing the metal part to detach. This may damage the centrifuge, destroy patient samples, and potentially expose lab staff to biohazardous material.

    Product
    PE Centrifuge, REF: B36365, a component of the Power Express
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V783000·2024-09-11

    2022-2023 Rivian R1T and R1S Defroster Defogger Software Failure Recall

    A software update may have deactivated the defroster and defogger on certain 2022-2023 Rivian R1T and R1S vehicles, reducing visibility and increasing crash risk. Rivian will release a free over-the-air software update.

    Product
    RIVIAN — 2022 RIVIAN R1T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2965-2024·2024-09-11

    Impella 5.5 Device Recalled for Missing Labeling on Catheter Interaction

    Abiomed is updating labeling for Impella 5.5 cardiac support pumps to include information about a potential device interaction with Shockwave Coronary IVL Catheters during coronary interventions.

    Product
    Impella 5.5 with SmartAssist S2 Set, US; Product Code: 1000100;
    Category
    Medical Device
    Distribution
    Distributed nationwide