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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13076–13100 of 89742

  • HighNHTSA·24V346000·2024-05-16

    2024 Jeep Grand Cherokee: Missing Bumper Foam May Prevent Airbag Deployment

    Certain 2024 Jeep Grand Cherokees may be missing foam in the front bumper, which could prevent the front airbags from deploying during a crash. Dealers will install the foam at no cost.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V347000·2024-05-16

    Custom Truck Recalls 2020 Ford F-550 for Electrical Fire Risk

    Custom Truck is recalling one 2020 Ford F-550 because a wiring fault may cause electrical circuits to overheat and increase fire risk.

    Product
    CUSTOM TRUCK & BODY WORKS — CUSTOM TRUCK & BODY WORKS FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24237·2024-05-16

    Kano Laboratories Recalls Super Lube Products for Non-Child-Resistant Packaging

    Kano Laboratories is recalling Super Lube Syncopen Synthetic Penetrant, Fire Resistant Hydraulic Fluid, and Metal Protectant and Corrosion Inhibitor products in sizes of five gallons or less because the packaging is not child-resistant as required by law, posing a poisoning risk to young children.

    Product
    Super Lube Syncopen Synthetic Penetrant, Super Lube Fire Resistant Hydraulic Fluid, and Super Lube Metal Protectant and Corrosion Inhibitor (consumer sizes of five gallons or less)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V349000·2024-05-16

    Mazda Recalls 2024 CX-90 Vehicles for Automatic Braking Defect

    Mazda is recalling 2024 CX-90 vehicles because the automatic emergency braking system may falsely detect objects, causing sudden braking and increasing crash risk.

    Product
    MAZDA — MAZDA CX-90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1231-2024·2024-05-15

    Chocolate Ice Cream Cookie Sandwiches Recalled for Undeclared Allergens

    Belgian Yummies recalls Chocolate Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens: milk, eggs, wheat, peanuts, and tree nuts. Consumers with allergies should not consume this product.

    Product
    Chocolate Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·24V342000·2024-05-15

    Morbark Brush Chippers Recalled for Fuel Line Fire Risk

    Alamo Group is recalling 2023-2024 Morbark brush chippers because fuel lines may lack the required pressure rating, creating a fire hazard.

    Product
    MORBARK — MORBARK EEGER BEEVER 1922, EEGER BEEVER 2131, EEGER BEEVER 1821
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V343000·2024-05-15

    Porsche Recalls 2024 718 Models Due to Shift Cable Installation Issue

    Porsche is recalling 2024 718 Cayman and Boxster vehicles because a safety clip may not be installed properly, potentially preventing the transmission from locking in park.

    Product
    PORSCHE — PORSCHE 718 CAYMAN, 718 BOXSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V345000·2024-05-15

    BMW 2024-2025 X5, X6, X7, XM, and Alpina XB7 Seat Belt Detection System Defect

    BMW recalls certain 2024-2025 X5, X6, X7, XM, and Alpina XB7 models due to a seat belt detection system defect that may fail to alert drivers of unbuckled passengers or allow proper deployment of the supplemental restraint system.

    Product
    BMW — BMW ALPINA XB7, X6, XM, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1233-2024·2024-05-15

    Belgian Yummies Salted Caramel Ice Cream Cookie Sandwiches recalled for undeclared allergens

    Belgian Yummies is recalling Salted Caramel Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens including milk, eggs, soy, wheat, peanuts, and tree nuts. The recall affects 254 units.

    Product
    Salted Caramel Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1230-2024·2024-05-15

    Vanilla Ice Cream Cookie Sandwiches Recalled for Undeclared Allergens

    Belgian Yummies is recalling Vanilla Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens: milk, eggs, wheat, peanuts, and tree nuts.

    Product
    Vanilla Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0485-2024·2024-05-15

    Prescription Drug Javygtor Recalled for Sub-Potency and Powder Discoloration

    Dr. Reddy's Laboratories is recalling Javygtor powder packets nationwide due to powder discoloration and sub-potency. The recall affects 17,332 cartons with multiple lot numbers.

    Product
    JAVYGTOR — JAVYGTOR (SAPROPTERIN DIHYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1609-2024·2024-05-15

    Insulin pump app may crash and drain battery, risking insulin delivery interruption

    Tandem's t:connect app version 2.7+ may crash repeatedly, draining the insulin pump battery faster than expected and potentially interrupting insulin delivery.

    Product
    t:connect mobile app used in conjunction with t:slim X2 insulin pump with Control-IQ technology
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V341000·2024-05-15

    Navistar Recalls 2024-2025 IC Bus School Buses for Brake Defect

    Navistar is recalling 2024-2025 IC Bus school buses because a faulty valve module may cause park brake failure or unexpected engagement.

    Product
    IC BUS — IC BUS CESB, CE SBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1234-2024·2024-05-15

    Key Lime Ice Cream Cookie Sandwiches Recalled for Undeclared Allergens

    Belgian Yummies is recalling Key Lime Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens: milk, eggs, soy, wheat, peanuts, and tree nuts. Consumers with these allergies should not consume the product.

    Product
    Key Lime Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1776-2024·2024-05-15

    Stealth S8 neurosurgical navigation software display error affecting surgical guidance

    Medtronic's Stealth S8 surgical navigation software has a display bug that may omit digits, letters, or decimals from critical readings during brain surgery. FDA classified this as Class I due to serious potential surgical errors.

    Product
    Stealth S8 Clinical Software Application, REF: 9735762, CE0344, Rx Only. Used in the StealthStation System as an aid for locating anatomical structures in either open or percutaneous neurosurgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1224-2024·2024-05-15

    D-LO's Pistachio Cheesecake Recalled for Undeclared Allergens and Food Coloring

    D-LO's Delightful Gourmet Cheesecake in pistachio flavor is being recalled due to undeclared wheat and soy allergens and undeclared food colors. The product poses a health risk to consumers with allergies to these ingredients.

    Product
    D-LO's Delightful Gourmet Cheesecake, Pistachio, 142g single serve UPC 8 60007 40398 9, and 678g six serving UPC 8 60007 40395 8, both serving sizes in clear plastic container with hinged lid
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1236-2024·2024-05-15

    Belgian Yummies ice cream recalled for undeclared milk and wheat

    Belgian Yummies Homemade Ice Cream Horchata Gelato distributed in Florida is recalled due to undeclared milk and wheat allergens that may affect consumers with allergies.

    Product
    Belgian Yummies Homemade Ice Cream Horchata Gelato. Packaged in 4.75 Liter gray pan.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1733-2024·2024-05-15

    Hologic BioZorb Bioabsorbable Markers Recalled for Adverse Events

    Hologic is recalling BioZorb Marker bioabsorbable surgical markers due to reported adverse events including infection, pain, device migration, and erosion. FDA classified this as Class I, affecting 53,492 units nationwide.

    Product
    BioZorb Marker-BioZorb 3D Bioabsorbable Marker-Intended Use radiographic marking of sites in soft tissue. 1) F0405 BioZorb Marker 4cm x 5cm 2) F0404 BioZorb Marker 4cm x 4cm 3) F0331 BioZorb Marker 1cm x 3cm x 3cm 4) F0231 BioZorb Marker 1cm x 3cm x 2cm 5) F0221 BioZorb…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1730-2024·2024-05-15

    Vyaire Twin Tube Sample Line Nozzle Separation Recall

    Vyaire Medical recalls Twin Tube sample line 240 cm devices (Model V-707327) due to potential nozzle separation during patient use. All lots manufactured prior to June 2023 are potentially affected.

    Product
    Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327; The TwinTube sample line 240cm is used in the Vyntus CPX. The TwinTube sample line 240cm is connected to the adapter for DVT. Twin Tube Probenschlauch (707004), which is sold outside the US only.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1232-2024·2024-05-15

    Raspberry Ice Cream Cookie Sandwich Recalled for Undeclared Allergens

    Belgian Yummies is recalling Raspberry Ice Cream Cookie Sandwiches distributed in Florida due to undeclared allergens including milk, eggs, wheat, peanuts, and tree nuts. Consumers with allergies should not consume these products.

    Product
    Raspberry Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1235-2024·2024-05-15

    Peanut Butter Ice Cream Cookie Sandwich Recalled: Undeclared Allergens

    Belgian Yummies is recalling Peanut Butter Ice Cream Cookie Sandwiches distributed in Florida due to undeclared milk, eggs, wheat, peanuts, and tree nuts. Consumers with allergies should not consume the product.

    Product
    Peanut Butter Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0486-2024·2024-05-15

    Sapropterin Dihydrochloride Powder for Oral Solution Recalled Due to Sub-Potency

    Dr. Reddy's Laboratories is recalling 2,402 cartons of Sapropterin Dihydrochloride Powder 100mg due to sub-potency associated with powder discoloration. The affected lot (T2200352) was distributed nationwide.

    Product
    Sapropterin Dihydrochloride Powder for Oral Solution 100mg, 30 individual packets per carton, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-477-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V340000·2024-05-15

    2025 MINI Countryman Rear Armrest May Detach During Airbag Deployment

    BMW is recalling 9 2025 MINI Countryman vehicles because the armrest support bracket on the rear side door panel may be improperly secured and detach during an airbag deployment, potentially striking occupants or interfering with airbag function.

    Product
    MINI — MINI COUNTRYMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0488-2024·2024-05-15

    Timolol Maleate ophthalmic solution recalled for defective container cap nozzle

    FDC Limited is recalling Timolol Maleate Ophthalmic Solution 0.5% distributed in New Jersey due to defective bottle caps with yellow spikes that can lodge in the nozzle, posing a risk of eye injury.

    Product
    TIMOLOL MALEATE — TIMOLOL MALEATE (TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0489-2024·2024-05-15

    TraMADol HCl 50 mg Tablets Recalled for Foreign Baclofen Tablets

    RemedyRepack Inc. is recalling TraMADol HCl 50 mg tablets nationwide after a pharmacist discovered a baclofen tablet in a tramadol bottle. Taking the wrong medication poses serious health risks.

    Product
    TraMADol HCl 50 mg Tablet, Packaged as (a) 30-count blister pack, NDC 70518-3824-00; (b) 90-count blister pack, NDC 70518-3824-02; (a) 180-count blister pack, NDC 70518-3824-03; RX ONLY, MFG: Advagen Pharma Limited, Plainsboro. NJ 08536, Repackaged by: RemedyRepack Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide