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 the agency’s own highest classification or reported deaths or serious injuries, 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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26076–26100 of 90145

  • SevereNHTSA·22V229000·2022-04-08

    Big Tex Recalls 2022 Trailers Due to Improperly Welded Couplers

    Big Tex Trailer Manufacturing is recalling 2022 50SR and 70SR trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.

    Product
    BIG TEX — BIG TEX 70SR, 50SR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V231000·2022-04-08

    Mercedes-Benz Recalls 21,306 Vehicles for Electrical Fire Risk

    Mercedes-Benz is recalling 21,306 vehicles because a ground cable bolt may not be secured properly, which can cause the electrical cable to overheat and increase the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS 450 4MATIC, AMG GLE53, GLE 450, GLE 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22C001000·2022-04-08

    CYBEX Sirona M Child Seat Recall for Foam Choking Hazard

    Columbus Trading-Partners USA is recalling CYBEX Sirona M child seats because loose foam pieces from the headrest pad may pose a choking hazard to children.

    Product
    CHILD SEAT:MATERIAL/PADDING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V232000·2022-04-08

    Mercedes-Benz 2018-2021 models recalled for rearview camera display failure

    Mercedes-Benz is recalling 126,443 vehicles from 2018-2021 because the rearview camera display may fail to show the rear view due to a software error, reducing visibility and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLB35, GLB 250, AMG CLA45, AMG CLA35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V230000·2022-04-08

    Western Star trucks recalled for failing windshield wiper linkages

    Daimler Trucks North America is recalling certain 2020-2022 Western Star 49X and 2021 Western Star 47X vehicles because windshield wiper linkages may break, causing wipers to fail and reducing visibility.

    Product
    WESTERN STAR — WESTERN STAR 47X, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22739·2022-04-07

    Bestar Wall Beds Recalled Due to Detachment and Crush Hazards

    Bestar wall beds can detach from the wall and fall, creating impact and crush hazards. One death and 60 additional injuries have been reported.

    Product
    Bestar Wall Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V227000·2022-04-07

    Western Star commercial trucks recalled for detaching hood air intake covers

    Daimler Trucks North America is recalling certain 2020-2023 Western Star trucks equipped with side air intakes on the hood. The stainless steel cover may loosen and detach, creating a road hazard and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR 57X, 49X, 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22738·2022-04-07

    biOrigins Sodium Hydroxide Products Recalled for Non-Child-Resistant Packaging

    CPSC recalls biOrigins sodium hydroxide products sold on Amazon from July 2020 through July 2021 due to non-child-resistant packaging and missing hazard label information. The product poses risk of chemical burns and skin/eye irritation to children.

    Product
    biOrigins Sodium Hydroxide Products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0959-2022·2022-04-06

    Cavendish Farms Frozen Hash Brown Patties Recalled for Undeclared Wheat and Barley

    Cavendish Farms is recalling Les Fermes Frozen Hash Brown Potato Patties because they contain undeclared wheat and barley flour. People with allergies to wheat or barley should not consume the product.

    Product
    Les Fermes Cavendish Farms Frozen Original Hash Brown Potato Patties Net Wt, 42.3 (1.2 kg). 12 retail packages per case, 20 patties per retail tray pack. UPC: 0 56210 34217 1
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0915-2022·2022-04-06

    Carbquik Mug Cake recalled due to undeclared milk allergen

    Tova Industries is recalling Carbquik Mug Cake Double Chocolate Chunk due to an undeclared milk allergen. Approximately 1,700 cases distributed through an Amazon distribution center in New Mexico are affected.

    Product
    Carbquik Mug Cake Double Chocolate Chunk, Net Wt. 9 oz 1.5oz packaged in foil pouch 6 servings per pouch, 24 pouches per case
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0912-2022·2022-04-06

    St. Benoit Yogurt Recalled for Undeclared Egg Allergen

    St. Benoit French Vanilla Yogurt is being recalled because it contains undeclared egg, a common allergen. Consumers with egg allergies should not consume the product.

    Product
    St. Benoit French Vanilla Yogurt; from pasture raised Jersey cows. Packaged in glass jar, net wt. 4.75 oz., UPC 6 49241 92910 9, St. Benoit Creamery. Sonoma, CA 95476 Certified Organic by CCOF
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0767-2022·2022-04-06

    Meclizine Hydrochloride Tablets Recalled Due to Incorrect Label Mix-up

    Jubilant Cadista Pharmaceuticals recalls Meclizine Hydrochloride Tablets with incorrect labeling. Bottles labeled as PredniSONE contain Meclizine, risking medication errors.

    Product
    MECLIZINE HYDROCHLORIDE — MECLIZINE HYDROCHLORIDE (MECLIZINE HYDROCLORIDE)
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Food)·F-0910-2022·2022-04-06

    Yogurt-Covered Raisins Recalled Nationwide Due to Undeclared Peanuts

    Multiple brands of yogurt-covered raisins distributed nationwide are being recalled due to undeclared peanuts. Consumers with peanut allergies face a serious health risk.

    Product
    Woody's Smokehouse brand Yogurt Raisins, 12.3 oz. (348g), clear plastic bag with front and back labels, UPC 0 95248 65531 0. Packed especially for Woody's Smokehouse Inc., Centerville, TX 75833, 903-536-9663, Woody's-Smokehouse.com Texas Best Smokehouse brand Yogurt Raisins, 8…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0913-2022·2022-04-06

    Taiwan Best Quality Enoki Mushrooms Recalled for Listeria monocytogenes Contamination

    Jan Fruits, Inc. is recalling Taiwan Best Quality Enoki Mushrooms (UPC 8 51084 00835 8) due to detection of Listeria monocytogenes. The product was distributed in California.

    Product
    Taiwan Best Quality Enoki Mushrooms; 200g/7.05 oz. clear plastic bag (50 bags/pcs per box). Product is in a clear bag with green bottom. UPC 8 51084 00835 8. Product of Taiwan Manufacturer: Changhua County Mushrooms Production Cooperative.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·22V220000·2022-04-06

    Lamborghini Recalls Huracan Models for Transmission Oil Defect

    Lamborghini is recalling 2020-2022 Huracan EVO and 2022 Huracan STO vehicles because insufficient transmission oil may cause clutch slippage or fire.

    Product
    LAMBORGHINI — LAMBORGHINI HURACAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V225000·2022-04-06

    Audi Recalls R8 Vehicles Due to Transmission Oil Deficiency

    Audi is recalling 2021-2022 R8 vehicles because insufficient transmission oil may cause clutch slippage or fire. Owners should contact dealers for a free inspection.

    Product
    AUDI — AUDI R8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0827-2022·2022-04-06

    Hand Pendant Malfunction in Proton Therapy Systems Poses Patient Injury Risk

    Mevion S250 and S250i Proton Therapy Systems hand pendants may malfunction, causing unintended motion of the therapy couch and nozzle. This poses a risk of patient injury if they contact moving equipment.

    Product
    Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N 10263 or P/N 37808)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2022·2022-04-06

    Radiation therapy planning software subject to jaw positioning errors during optimization

    RayStation radiation therapy planning software (versions 6-11A) may unexpectedly change jaw positions during optimization after dose or target modifications. Users should verify treatment plans carefully before delivery.

    Product
    TomoHelical and TomoDirect plans in RayStation 6, 7, 8A, 8B, 9A, 9B, 10A, 10B and 11A. Build Numbers: 6.1.1.2, 6.2.0.7, 6.3.0.6, 7.0.0.19, 8.0.0.61, 8.0.1.10, 8.1.0.47, 8.1.1.8, 8.1.2.5, 9.0.0.113, 9.1.0.933, 9.2.0.483, 10.0.0.1154, 10.0.1.52, 10.1.0.613, 11.0.0.951 or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0737-2022·2022-04-06

    Lansoprazole Capsules Recalled for Failed Dissolution in Stability Testing

    Dr. Reddy's Laboratories is recalling specific lots of Lansoprazole 15 mg delayed-release capsules nationwide because the capsules failed to dissolve properly during long-term stability testing, which could affect medication effectiveness.

    Product
    LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0734-2022·2022-04-06

    Testosterone Cypionate Injectable Vials Recalled for Lack of Sterility Assurance

    Drug Depot, Inc. is recalling 24 vials of Testosterone Cypionate 200 MG/ML Injectable nationwide due to lack of sterility assurance. The product was distributed throughout the USA and Puerto Rico.

    Product
    TESTOSTERONE CYPIONATE *GS* Oil 200 MG/ML Injectable, Packaged in a multi dose 10ML vial, Formula ID 76681, APS Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0850-2022·2022-04-06

    Medical software recall: RayStation radiation therapy dose calculation errors

    RayStation and RayPlan radiation therapy planning software may calculate incorrect radiation doses due to a source-to-skin distance calculation error. The FDA Class II recall affects 149 units distributed in the US.

    Product
    RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5 Service Pack 2 (5.0.2.35), RayStation 5 Service Pack 3 (5.0.3.17), RayStation 6/RayPlan 2 (6.0.0.24), RayStation 6/RayPlan 2 Service Pack 1 (6.1.1.2)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0852-2022·2022-04-06

    Hanger-Bar 2P 45cm Recalled for Fall Hazard from Loosened Set Screw

    Human Care USA, Inc. is recalling the Hanger-Bar 2P 45cm because the set screw may loosen due to a manufacturing defect, creating a fall hazard.

    Product
    Hanger-Bar 2P 45cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0829-2022·2022-04-06

    Liko Universal Twinbar 670 QRH Patient Lift Accessory Recalled for Fall Risk

    Baxter Healthcare Corporation is recalling 1,399 Liko Universal Twinbar 670 QRH patient lift accessories due to an incorrect center bolt used during assembly. The defect could cause a patient to fall during use.

    Product
    Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087.
    Category
    Medical Device
    Distribution
    Distributed nationwide