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.

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3326–3350 of 89480

  • HighFDA (Devices)·Z-1257-2026·2026-02-11

    Urinalysis test strips recalled over missing FDA premarket clearance

    Changchun Wancheng Bio-Electron is recalling 91,366 units of LotFancy Urinary Tract Infection Urine (UTI) Test Strips because tests requiring a 510(k) were distributed before they could be legally marketed.

    Product
    LotFancy Urinary Tract Infection Urine (UTI) Test Strips; PALINOIA UTI-10 PARAMETER REAGENT STRIPS; Vaunn Medical 8-in-1 Urinalysis Reagent Strip; JNW Direct 4-in-1 UTl Urinalysis Test Strips; Urinify STRENGTH; Urinify ESSENTIAL, Urinify Urinary Tract Infection (UTI)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1248-2026·2026-02-11

    Subretinal injection cannulas recalled over voids in pouch seals

    Vortex Surgical is recalling 14,789 units because there may be voids in the seal of the Tyvek pouches, which compromises the sterile barrier.

    Product
    25GA Subretinal Injection Cannula VS0220.25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1299-2026·2026-02-11

    X-ray systems recalled over welded contactor contacts that may overheat

    FUJIFILM Healthcare Americas is recalling 16 FDR Visionary Suite systems because welded contactor contacts may keep supplying current after the device is switched off.

    Product
    FDR Visionary Suite; Model Number: CH-200; Version: (1) 566-16130-23, (2) 566-16130-31, (3)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1267-2026·2026-02-11

    Vivoo sodium and hydration tests recalled over missing premarket clearance

    Changchun Wancheng Bio-Electron is recalling 3,300 units of Vivoo Sodium Test because tests requiring a 510(k) were distributed before they could be legally marketed.

    Product
    Vivoo Sodium Test; Vivoo Vitamin C Test; Vivoo Hydration Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0482-2026·2026-02-11

    Frozen half shell oysters recalled over potential norovirus contamination

    Khee Trading is recalling 7,306 cases of frozen half shell oysters imported from the Republic of Korea over potential norovirus contamination.

    Product
    Product is Frozen Half Shell Oysters in 15-16 pound blocks. Packaged in generic brown cardboard boxes. Side panel reads: HAFL SHELL OYSTER Spec: 144PCS; Imported by: Khee Trading Inc., Compton, CA Side panel reads: Method of harvest: Farm Raised Country of Origin: Republic of Kor
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1258-2026·2026-02-11

    Ketone and urinalysis strips recalled over missing premarket clearance

    Changchun Wancheng Bio-Electron is recalling 32,500 units covering The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips because tests requiring a 510(k) were distributed before they could be legally marketed.

    Product
    The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips; URIMED Urinalysis Reagent Strips URS-5, Rapid UTI Test Includes Ketones: Leukocytes, Nitrite, pH, Ketone, Protein; Vivoo Ketone Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26T006000·2026-02-10

    Vee Tyre Recalls Taiga AT Tires Due to Sidewall Separation Risk

    Vee Tyre is recalling specific Taiga AT tires because the sidewall and inner liner may crack and separate, increasing the risk of a crash.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V076000·2026-02-10

    2024–2027 Volvo VNL (4) trucks recalled for inadequate parking brake

    Volvo Trucks is recalling certain 2024–2027 VNL (4) vehicles lacking auxiliary parking brakes, which can result in inadequate parking brake force and rollaway risk.

    Product
    VOLVO — VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V075000·2026-02-09

    Harley-Davidson Sportster S upper triple clamp may fracture during use

    Harley-Davidson is recalling certain 2021-2026 RH1250S Sportster S motorcycles because the upper triple clamp may fracture, which can lead to a loss of control.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON RH1250S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V074000·2026-02-08

    Oshkosh Recalls 2025-2026 NGDV Vehicles Due to Brake Pedal Defect

    Oshkosh is recalling 2025-2026 NGDV and NGDV Electric vehicles because the brake pedal mounting pin and clip may be missing, risking loss of braking ability.

    Product
    OSHKOSH — OSHKOSH NGDV ELECTRIC, NGDV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V072000·2026-02-06

    Volvo Recalls 2017 S60L Vehicles Due to Door Latch Defect

    Volvo is recalling 2,758 2017 S60L vehicles because a door latch component may break, preventing the door from latching securely and increasing injury risk.

    Product
    VOLVO — VOLVO S60L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V073000·2026-02-06

    Mercedes-Benz EQB high voltage battery may fail internally and catch fire

    Mercedes-Benz is recalling certain 2022-2024 EQB vehicles because the high voltage battery may fail internally and lead to a vehicle fire while parked or driving. Owners are advised to park outside.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQB 350 4MATIC, EQB 300 4MATIC, EQB 250+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V070000·2026-02-06

    Mercedes-Benz Metris air bag control unit may accumulate water

    Daimler Vans USA is recalling certain 2020 and 2022-2023 Mercedes-Benz Metris right-hand-drive vehicles because water may accumulate on the air bag control unit and stop the air bags deploying as intended.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V067000·2026-02-05

    Jaguar I-PACE high voltage battery may overheat increasing fire risk

    Jaguar is recalling certain 2020-2021 I-PACE vehicles because the high voltage battery may overheat. Owners are advised to park and charge outside and limit charging to 90%.

    Product
    JAGUAR — JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26250·2026-02-05

    PurSteam steamers recalled after reports of burns from expelled hot water

    About 75,400 PurSteam Elite Travel Steamers and about 119,000 PurSteam Mighty Lil Steamers are being recalled because they can expel hot water from the steam nozzle during use.

    Product
    PurSteam Mighty Lil Steamers and PurSteam Elite Travel Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26253·2026-02-05

    Outdoor chairs and barstools recalled after reports of legs bending

    About 158,486 Lancaster Table & Seating powder-coated aluminum outdoor chairs and barstools are being recalled because the legs can bend or break while in use.

    Product
    Lancaster Table & Seating Powder-Coated Aluminum Outdoor Chairs and Barstools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26256·2026-02-05

    Ammunition desiccant tiles recalled over failure to control humidity

    About 760 Ammo Tabs fiber desiccant tiles are being recalled because they can fail to protect firearms and ammunition from humidity, allowing corrosion or rust.

    Product
    Ammo Tabs Fiber Desiccant Tiles used for Firearms and Ammunition
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26248·2026-02-05

    Seven drawer dressers recalled over tip-over and entrapment hazards

    About 2,900 Fixwal 7-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.

    Product
    Fixwal 7-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide