The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

6601–6625 of 89512

  • HighFDA (Devices)·Z-1992-2025·2025-06-25

    Fresenius 5008X HDF Hemodialysis Blood Tubing Sets recalled for potential blood leaks

    Fresenius Medical Care is recalling 5008X HDF Hemodialysis Blood Tubing Sets due to potential blood leaks between the venous chamber and tubing. The recall affects hemodialysis, hemodiafiltration, hemofiltration, and isolated ultrafiltration procedures nationwide.

    Product
    5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline, Model Number: 03-5100-7. b. 5008X Standard HDF Bloodline w/CLIC, Model Number: 03-5100-7C. c. 5008X Standard HDF Bloodline w/ Twister, Model Number: 03-5150-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0048-2025·2025-06-25

    Topo Chico Mineral Water Recalled for Pseudomonas Contamination

    The Coca-Cola Company is recalling Topo Chico Mineral Water 16.9 fl oz bottles due to potential Pseudomonas contamination. Product was distributed to Arizona, Louisiana, New Mexico, Nevada, and Texas.

    Product
    Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle UPC 0 21136 18061 9, Case UPC 0 21136 18062 6 MADE IN MEXICO BY: CIA. TOPO CHICO, S. DE R.L. DE C.V. MONTERREY NO. 6500 COL. TOPO CHICO, MTY.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1980-2025·2025-06-25

    Portable Oxygen Concentrator with Erroneous Calibration Values

    Ohio Medical Corporation is recalling 36 units of the GCE HEALTHCARE Zen-O lite portable oxygen concentrator due to erroneous calibration values that may cause the device's alarm for low oxygen purity to function incorrectly as the device ages.

    Product
    GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1977-2025·2025-06-25

    Fitbone Trochanteric Nail may bend during insertion and require replacement

    Orthofix Srl is recalling Fitbone Trochanteric Nails (Lot B4771336 and B4771337) because the implant may bend at the distal tail during insertion, potentially requiring replacement.

    Product
    REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0055-2025·2025-06-25

    Fruit and Veg Tray 64oz Recalled for Potential Salmonella Contamination

    GBC Food Services, LLC is recalling Fruit and Veg Tray 64oz products due to potential Salmonella contamination. The affected products were distributed to multiple states and purchased between May 8 and May 21, 2025.

    Product
    Fruit and Veg Tray 64oz 850065403748 Purchase Dates: 05/08/2025 to 05/21/2025
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1982-2025·2025-06-25

    Siemens UROSKOP Omnia Max frequency inverter fire risk recalled

    Siemens is recalling UROSKOP Omnia Max medical devices due to a resistor in the frequency inverter that may overheat and ignite the plastic housing. Twenty-five units distributed nationwide are affected.

    Product
    UROSKOP Omnia Max. Model Number: 10762473
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1987-2025·2025-06-25

    Biomet 3i Certain-Compatible 4.1mm Milled Titanium Dental Abutments

    Preat Corp is recalling Biomet 3i Certain-compatible 4.1mm Milled Titanium Abutments (Model 9001767-F) due to manufacturing defects that may cause improper screw engagement. The screw seat was positioned too high, potentially compromising the attachment of mating screws to the underlying implant.

    Product
    Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V380000·2025-06-23

    GEM Recalls 2022-2025 Electric Vehicles Due to Ball Joint Separation Risk

    GEM is recalling 2022-2025 e2, e4, e6, and eLXD vehicles because improperly tightened fasteners may cause the front lower ball joint to separate, potentially leading to a loss of steering control.

    Product
    GEM — GEM E4, E6, ELXD, E2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V326000·2025-06-23

    Western Star battery to starter stud can short circuit

    Daimler Trucks is recalling certain 2020-2026 Western Star 49X and 2021-2026 47X vehicles because a stud connecting the battery to the starter at the frame rail may have been incorrectly installed.

    Product
    WESTERN STAR — WESTERN STAR 47X, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V384000·2025-06-23

    Keystone Recalls 2025 Toy Haulers Due to Missing Rear Gate Pins

    Keystone is recalling 2025 Carbon, Fuzion, and Raptor toy haulers because missing rear gate pins or leg support brackets may allow the gate to shift, increasing injury risk.

    Product
    KEYSTONE — KEYSTONE FUZION, RAPTOR, CARBON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V425000·2025-06-20

    Travel trailer patio door transit latch cannot be opened from inside

    Forest River is recalling certain 2025-2026 Wildwood and Salem travel trailers because the exterior transit latch on the rear patio door cannot be unlocked from inside the vehicle.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V423000·2025-06-20

    2026 Forest River Spirit travel trailers recalled for defective safety chains

    Forest River is recalling certain 2026 Spirit travel trailers because the installed safety chains may not meet the actual Gross Vehicle Weight Rating, posing a risk of trailer separation from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER SPIRIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V424000·2025-06-20

    2026 Forest River Sabre Fifth Wheel Griddle Fire Risk Recall

    Forest River is recalling 2026 Sabre fifth wheel recreational trailers because the exterior griddle may be incorrectly installed, allowing it to be stowed while still connected to LPG, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER SABRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-06202025-01·2025-06-20

    USDA Issues Public Health Alert for Uninspected Thompson's Meat Sauce Products

    USDA FSIS issued a public health alert for Thompson's meat sauce products produced without federal inspection. Consumers in Illinois and Indiana are urged to discard the items.

    Product
    FSIS Issues Public Health Alert for Meat Sauce Products Produced Without the Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·25V422000·2025-06-19

    Honda Recalls 2013 Accord Vehicles for Driveshaft Corrosion Risk

    Honda is recalling 2013 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because the driveshaft may corrode and break, potentially causing a loss of drive power or vehicle rollaway.

    Product
    HONDA — HONDA ACCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V419000·2025-06-19

    Subaru Forester child seat anchor bolts may come loose

    Subaru is recalling certain 2025 Forester vehicles because the child seat anchor bolts may have been improperly tightened, allowing them to come loose.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V385000·2025-06-19

    Vanguard Recalls 2021-2023 VXP Trailers Due to Hook Box Defect

    Vanguard is recalling 2021-2023 VXP 28-Foot Pup trailers because the pintle hook box assembly may crack or break, reducing stability while being towed.

    Product
    VANGUARD — VANGUARD VXP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V405000·2025-06-19

    Shyft Recalls 2024-2025 Utilimaster Aeromaster for Camera Display Defect

    Shyft Group is recalling 2024-2025 Utilimaster Aeromaster vehicles because the 360-degree camera monitor may not display the correct image at startup, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V421000·2025-06-19

    Supreme Recalls 2025 Wabash Trucks Due to Liftgate Pin Seizure Risk

    Supreme is recalling 2025 Wabash trucks because insufficient lubrication on the liftgate pin may cause it to seize, leading to liftgate failure and injury risk.

    Product
    SUPREME — SUPREME WABASH TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1865-2025·2025-06-18

    Z-800 Infusion System recalled for unverified software installation

    Zyno Medical LLC is recalling 613 units of the Z-800 Infusion System distributed nationwide because unreleased software versions were installed on the devices without verification or validation.

    Product
    Z-800 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-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