The Recall Desk

State

Virginia product recalls

72,820 recalls have nationwide distribution and so reach Virginia. 9,476 additional recalls listed Virginia specifically in their distribution scope.

What the numbers show

Total
9,476
Critical
1,285
Severe
2,291
Most recent
2026-09-02

Of the 9,476 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 2,291 (24%) are Severe.

These figures cover only the 9,476 recalls whose distribution notice names Virginia specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

326–350 of 82296

  • HighCPSC·26691·2026-08-13

    Deli Jerry Fuel Containers Recalled Due to Burn Hazard and Child Poisoning Risk

    Deli Jerry fuel containers sold on Walmart.com are recalled because their caps are not child-resistant, posing burn and poisoning risks to children. No injuries have been reported; consumers should stop using them and contact Deli OfficeSupplies for a refund.

    Product
    Deli Jerry Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26698·2026-08-13

    CuberShop Magnetic Speed Cubes Recalled Over Magnet Ingestion Hazard

    CuberShop Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) are recalled because loose high-powered magnets in the packaging pose an ingestion hazard to children. No injuries have been reported.

    Product
    CuberShop Magnetic Stickerless Speed Cubes, model YJ MGC 5×5
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V529000·2026-08-13

    Chrysler Recalls 2026 Jeep Grand Cherokee Models for Wiper Software Issue

    Chrysler is recalling 81 2026 Jeep Grand Cherokee and Grand Cherokee L vehicles because a software issue may cause windshield wipers to fail, reducing visibility.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND CHEROKEE L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26690·2026-08-13

    DUMOS Nine-Drawer Dressers Recalled for Tip-Over and Entrapment Hazards

    DUMOS Nine-Drawer Dressers are recalled because they can tip over and entrap children if not anchored to the wall, violating the STURDY Act. Consumers should stop using unanchored units and contact DUMOS for a full refund.

    Product
    DUMOS Nine-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V531000·2026-08-13

    Chrysler Recalls 2026-2027 Vehicles for Rearview Camera Display Failure

    Chrysler is recalling 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles because the rearview camera image may fail to display when reversing, increasing crash risk.

    Product
    RAM — RAM, CHRYSLER, JEEP PROMASTER BEV, PACIFICA, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26702·2026-08-13

    Hampton Bay 52-Inch Ceiling Fans Recalled Over Blade Separation Hazard

    Hampton Bay Halwin 52-inch ceiling fans are being recalled because the fan blades can separate from the motor flywheel, posing impact and injury risks. About 9,460 units sold at Home Depot between January 2023 and October 2025 are affected.

    Product
    Hampton Bay Halwin 52-inch Indoor/Outdoor Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26697·2026-08-13

    Shengsen Prank Sound Makers Recalled Over Battery Ingestion Risk

    Shengsen Prank Sound Makers are recalled because the lithium coin batteries can be easily accessed by children, posing an ingestion hazard. About 667 units sold on Amazon from April 2024 through April 2026 are affected.

    Product
    Shengsen Prank Sound Maker
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0743-2026·2026-08-12

    Cyclophosphamide Injection Recalled Due to Stainless Steel Particulate Matter

    Sunny Pharmtech Inc. is recalling 4,077 vials of Cyclophosphamide for Injection due to stainless steel particulate matter found in the product. The recall affects vials distributed nationwide in the USA.

    Product
    Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2796-2026·2026-08-12

    Halyard convenience kits recalled due to potential particulates in manifolds

    AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2797-2026·2026-08-12

    Halyard Convenience Kits Recalled Due to Particulates in Manifolds

    AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY SAMM066-15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1207-2026·2026-08-12

    Clover Hill Dairy Cheese Variety Recalled for Listeria Contamination

    Clover Hill Dairy, LLC is recalling its Mild Cheese Variety (3-in-a-pack assorted White Colby, Marble Jack, Yummy Cheddar) because the product may be contaminated with Listeria monocytogenes. The recall affects products distributed in MD, VA, and NY.

    Product
    Clover Hill Dairy LLP, Mild Cheese Variety (3-in-a-pack assorted White Colby, Marble Jack, Yummy Cheddar). Sold in approximate 0.20-lb (3.2oz) units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2876-2026·2026-08-12

    GE Healthcare MAC VU360 Electrocardiograph Software Recall

    GE Healthcare is recalling 163 MAC VU360 electrocardiograph units due to a software issue that may cause a previous patient's data to remain visible and be incorrectly associated with a subsequent patient.

    Product
    GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1199-2026·2026-08-12

    Clover Hill Dairy Soft Ricotta Recalled Due to Listeria Contamination

    Clover Hill Dairy is recalling Soft Ricotta and Soft Ricotta with Jalapenos due to Listeria monocytogenes contamination. Products were distributed in MD, VA, and NY.

    Product
    Clover Hill Dairy LLP, Soft Ricotta (Requeson), and Soft Ricotta with Jalapenos (Requeson Con Chile). Sold in 2- and 5-gallon buckets, and 10oz, 12oz, and 14oz individually packaged food grade clamshell containers. The 5- and 2-gallon buckets are shrink wrapped. Keep refrigerated
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2862-2026·2026-08-12

    Stryker AHTO Tube Set Packaging Recalled for Handpiece Leaking

    Stryker is recalling 46,212 units of its AHTO Tube Set Packaging (Catalog Number 0250070600) due to reported complaints of leaking from the handpiece during use. The recall affects products distributed worldwide, including US Nationwide and multiple countries.

    Product
    STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2875-2026·2026-08-12

    Merge OrthoPACS Imaging Workstation Recall for Patient Data Display Issue

    Merge Healthcare is recalling 5 units of its Merge OrthoPACS medical imaging diagnostic workstation due to a software issue where thumbnails from a previously opened patient study may appear while a different patient study is currently open.

    Product
    Merge OrthoPACS, medical imaging diagnostic workstation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2856-2026·2026-08-12

    Powered Wheelchair Control Software Recall by munevo

    Munevo is recalling 19 powered wheelchair hands-free control systems due to a software issue that may cause the driving mechanism to fall out of calibration, leading to unexpected steering drift or imprecise control.

    Product
    munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2850-2026·2026-08-12

    Quantum Rehab Q6 Edge 4 Wheelchairs Recalled Due to Controller Software Issue

    Pride Mobility Products Corp. is recalling Quantum Rehab Q6 Edge 4 powered wheelchairs because a software issue can cause unexpected braking and potential injury.

    Product
    Brand Name: Quantum Rehab Product Name: Q6 Edge 4 Model/Catalog Number: Q6 Edge 4 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1208-2026·2026-08-12

    Fresh Cheddar Curd Cheese Recalled Due to Listeria Contamination

    Clover Hill Dairy's Fresh Cheddar Curd cheese is recalled due to Listeria monocytogenes contamination. The product was distributed in Maryland, Virginia, and New York.

    Product
    Clover Hill Dairy LLP, mild cheese variety (Fresh Cheddar Curd). Sold in approximate 0.75-lb and 1.5-lb box units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2897-2026·2026-08-12

    United Orthopedic U2 Knee Implant Bushings Recalled Over Engraving Design Issue

    United Orthopedic Corp. is recalling three Femoral offset bushing components of the U2 Total Knee System due to a design issue causing incorrect engraved numbering that could lead to incorrect implant orientation during surgery.

    Product
    Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No, N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1218-2026·2026-08-12

    Salvadorean Cheese Recalled for Possible Listeria Contamination

    La Colonia Foods LLC is recalling Selectos Latinos Requeson Salvadoreno Ricotta Style Salvadorean Cheese (14 oz) due to possible contamination with Listeria monocytogenes.

    Product
    Selectos Latinos Requeson Salvadoreno Ricotta Style Salvadorean Cheese, Net Weight 14 oz, packed into retail-sized clear plastic containers. Keep refrigerated.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0745-2026·2026-08-12

    FDA Recalls Mirabegron Tablets Over Nitrosamine Impurity

    Zydus Pharmaceuticals is recalling Mirabegron extended-release tablets, 25 mg, due to an out-of-specification result for the N-Nitroso Mirabegron impurity. The recall affects nationwide distribution in the USA.

    Product
    MIRABEGRON — MIRABEGRON (MIRABEGRON)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1215-2026·2026-08-12

    Clover Hill Dairy Pepper Jack Cheese Varieties Recalled Due to Listeria Contamination

    Clover Hill Dairy, LLC is recalling Pepper Jack Cheese Varieties due to potential Listeria monocytogenes contamination.

    Product
    Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (3-in-a-Pack Assorted Jalapeno Cheddar, Pepper Jack, Sizzling Colby). Sold in approximate 0.20-lb (3.2oz) units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2843-2026·2026-08-12

    Powered Wheelchair Controller Software Recall by Pride Mobility

    Pride Mobility is recalling 1,102 Q6 Edge 3 Stretto powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.

    Product
    Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Stretto Model/Catalog Number: Q6 Edge 3 Stretto Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1200-2026·2026-08-12

    Smoked Pepper Cheese Varieties Recalled Due to Listeria monocytogenes Contamination

    Clover Hill Dairy, LLC is recalling Smoked Pepper Cheese Varieties (Jalapeno Cheddar) because they may be contaminated with Listeria monocytogenes.

    Product
    Clover Hill Dairy LLP, Smoked Pepper Cheese Varieties (Jalapeno Cheddar), sold in 1/2-lb and 1-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states