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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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

16401–16425 of 89775

  • HighFDA (Devices)·Z-0208-2024·2023-11-08

    POC Analyzer Risk of Erroneous Creatinine Results During Cartridge Startup

    Nova Biomedical's Stat Profile Prime Plus POC analyzer may report inaccurate creatinine results during the first 2-4 hours after sensor cartridge installation. Standard quality control checks may not detect these errors.

    Product
    Nova Stat Profile Prime Plus POC Analyzer (CE)-Intended to measure certain gases in blood, serum, plasma or pH of blood, serum, and plasma. (1) PN 63368 Stat Profile Prime Plus POC Analyzer (2) PN 63369 Stat Profile Prime Plus POC Analyzer, Remanufactured P/N: 57400…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0314-2024·2023-11-08

    Crush Orange Soda Recalled Due to Plastic Foreign Material

    Pepsi Beverages is recalling Crush Orange Soda 24-packs due to plastic foreign material found in some cans. The recall affects 184 cases distributed in Minnesota with lot code JUL2924XXXXMC10243 and a best-by date of July 29, 2024.

    Product
    Crush Orange Soda, 24 Pack. 24 - 12 oz. cans. Caffeine Free. Contains No Juice. UPC 0 78000-01309 2. Produced under the Authority of Dr Pepper/Seven Up, Inc., 6425 Hall of Fame Lane, Frisco, TX 75034
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0081-2024·2023-11-08

    Gynazole 1 Butoconazole Vaginal Cream Recalled for Formulation Error

    Padagis US LLC is recalling Gynazole 1 butoconazole nitrate vaginal cream nationwide due to a manufacturing error where hydrophilic colloidal silica was used instead of hydrophobic colloidal silica.

    Product
    GYNAZOLE 1 — GYNAZOLE 1 (BUTOCONAZOLE NITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0206-2024·2023-11-08

    Oncology Information System Document Values Not Visible in Read-Only Mode

    RayCare oncology information system versions 5B and 6A contain a software bug where document field values do not display when documents are opened in read-only mode outside the Documents workspace.

    Product
    RayCare 5B and 6A including service packs- An oncology information system used to support workflows and scheduling, as well as clinical information, planning and treatment management for oncology care Product name (build number): (1)RayCare 5B SP1 (5.1.1.60246); (2)RayCare…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0216-2024·2023-11-08

    Cepheid Xpert Xpress Strep A test kits may produce invalid results

    Cepheid is recalling 1,413 Xpert Xpress Strep A test kits due to a defect in the included pipettes. Defective pipettes may fail to dispense adequate sample volume, resulting in invalid test results or no test result.

    Product
    Xpert Xpress Strep A, REF:Xprstrepa-CE-10, CE IVD,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V748000·2023-11-07

    Alexis Fire Equipment Recalls Fire Apparatus Due to Parking Brake Defect

    Alexis Fire Equipment is recalling 2021-2024 Fire Apparatus vehicles because a defect in the inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V746000·2023-11-07

    Mack Recalls 2024 MD Trucks Due to Steering Wheel Bolt Issue

    Mack Trucks is recalling 2024 MD trucks because the steering wheel attachment bolt may loosen and separate, potentially causing the steering wheel to detach.

    Product
    MACK — MACK MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E086000·2023-11-07

    Cruise Recalls 950 Vehicles for Automated Driving System Software Defect

    Cruise LLC is recalling 950 vehicles because a software defect in the Collision Detection Subsystem may cause the vehicle to move after a crash.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V747000·2023-11-07

    Spartan Fire Emergency Vehicles Recalled for Parking Brake Defect

    Custom Fire Apparatus is recalling 2021-2024 Spartan emergency vehicles because a parking brake defect may allow unintentional movement, increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, FC-94, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V749000·2023-11-07

    Peterbilt Recalls 2024 520 Trucks Due to Engine Bracket Risk

    PACCAR is recalling 2024 Peterbilt 520 vehicles because a rear lifting bracket may detach, posing an injury risk during engine lifting.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V744000·2023-11-06

    2024 Buick Envista Software Update: Instrument Panel Display Blanking Issue

    General Motors recalls certain 2024 Buick Envista vehicles for a software defect that may cause the instrument panel display to go blank, preventing visibility of critical safety information like vehicle speed and warning lights.

    Product
    BUICK — BUICK, CHEVROLET ENCORE GX, TRAX, ENVISTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·057-2023·2023-11-04

    Tyson Recalls Chicken Patties Due to Possible Metal Contamination

    Tyson Foods is recalling approximately 29,819 pounds of fully cooked chicken patties that may contain metal pieces. The recall affects specific lot codes distributed to nine states.

    Product
    Tyson Foods, Inc. — Tyson Foods Inc. Recalls Chicken Patty Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    9 states
  • HighNHTSA·23V743000·2023-11-03

    Tesla Model S and Model X Incorrect Air Bag Recall

    Tesla is recalling 2021-2024 Model S and Model X vehicles because an incorrect air bag was installed when the steering wheel was replaced. The incompatible air bag could deploy incorrectly during a crash, increasing the risk of injury.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V739000·2023-11-03

    Forest River Travel Trailers Electrical Wire Gauge Defect Recall

    Forest River is recalling 2023-2024 Sandstorm, Stealth, and 2024 Shockwave travel trailers. The electrical wire from the 50-amp inlet has incorrect gauge and may melt, creating a fire hazard.

    Product
    FOREST RIVER — FOREST RIVER SHOCKWAVE, SANDSTORM, STEALTH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V742000·2023-11-03

    Gulf Stream Recalls 2024 Travel Trailers with Incorrect Tire Certification Labels

    Gulf Stream is recalling 2024 travel trailers because incorrect tire size and pressure information on the Federal certification label may lead to overinflation and loss of vehicle control.

    Product
    GULF STREAM — GULF STREAM FRIENDSHIP, AMERI-LITE, INDEPENDENCE, CONQUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·056-2023·2023-11-02

    Fairmont Foods Recalls Frozen Spaghetti Loops for Undeclared Egg Allergen

    Fairmont Foods is recalling approximately 147,132 pounds of frozen spaghetti loops with meat sauce due to misbranding and an undeclared egg allergen.

    Product
    Fairmont Foods, Inc. — Fairmont Foods, Inc., Recalls Frozen Spaghetti Loops With Meat Sauce Entree Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·23V737000·2023-11-02

    Freightliner M2 and 114SD Recall for Engine Lifting Bracket Defect

    Daimler Trucks North America is recalling 2024 Freightliner M2 and 114SD vehicles because an engine lifting bracket may detach, posing an injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER M2, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V735000·2023-11-02

    2023-2024 Honda Pilot steering rack defect may cause loss of steering control

    Honda is recalling certain 2023-2024 Pilot vehicles due to a loose ball bearing in the steering rack gearbox assembly. This defect can result in loss of steering control or steering lock-up, increasing crash risk.

    Product
    HONDA — HONDA PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24017·2023-11-02

    Yoocaa baby loungers recalled for suffocation and entrapment hazards

    Yoocaa baby loungers fail to meet CPSC safety requirements for infant sleep products, posing suffocation, fall, and entrapment risks. About 4,140 units sold on Amazon from January 2021 through May 2023 are affected; no injuries have been reported.

    Product
    Yoocaa baby loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide