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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15901–15925 of 89775

  • HighFDA (Food)·F-0475-2024·2023-12-06

    Le Croissant Turkey & Cheddar Sandwich Recalled for Undeclared Milk and Soy

    Le Croissant Turkey & Cheddar sandwiches are being recalled due to undeclared milk and soy allergens. The product was distributed across 15 states.

    Product
    Le Croissant Turkey & Cheddar Net Wt. 5.5oz (156g) UPC:766375261629 Packaged in clamshell container. Sold as single unit and 6-unit pack under Food Unlimited brand
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0474-2024·2023-12-06

    Food Unlimited Ham & Swiss Recalled for Undeclared Milk and Soy

    Food Unlimited-brand Le Croissant Ham & Swiss sandwiches are being recalled due to undeclared milk and soy allergens. Affected products distributed across multiple states should not be consumed by people with these allergies.

    Product
    Le Croissant Ham & Swiss Net Wt. 5.5oz (156g) UPC:766375261612 Packaged in clamshell container. Sold under Food Unlimited brand.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0470-2024·2023-12-06

    Frito-Lay Chickpea Veggie Crisps recalled for undeclared milk allergen

    Frito-Lay is recalling 16,100 bags of Chickpea Veggie Crisps (UPC 02840020646) due to undeclared milk allergen. Consumers with milk allergies should not consume the product.

    Product
    Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0404-2024·2023-12-06

    Medical Device Recall: SENTIERO Hearing Screening Devices for Technical Distortions

    PATH's SENTIERO SCREENING hearing examination devices (Model SOH100098) are being recalled due to technical distortions that may exceed expected levels. The recall affects devices distributed in Florida, Missouri, Ohio, and Wisconsin.

    Product
    SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-0477-2024·2023-12-06

    Diet Coke 12oz aluminum cans 12-pack recalled for potential foreign material

    Diet Coke 12oz aluminum cans sold in 12-pack fridge packs are being recalled due to potential foreign material. The recall affects 417 cases with specific lot numbers distributed to Alabama, Florida, and Mississippi.

    Product
    Diet Coke packaged in 12oz aluminum cans - 12 pack fridge pack
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0419-2024·2023-12-06

    Olympus EVIS EXERA III Colonoscope Recall for Connector Defect

    24 Olympus EVIS EXERA III colonoscopes distributed to six states are recalled due to improperly repaired connectors that may cause image loss, decreased suction, or improper reprocessing, potentially exposing patients to contaminated equipment.

    Product
    PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0423-2024·2023-12-06

    RAPIDPOINT 500 Blood Gas System: Drug Interference May Cause False Sodium Readings

    Siemens RAPIDPOINT 500 Blood Gas System may produce falsely elevated sodium results due to drug interference from Perhexiline Maleate or Atomoxetine Hydrochloride. This could lead to missed hyponatremia or inappropriate treatment of hypernatremia.

    Product
    RAPIDPOINT 500 Blood Gas System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0422-2024·2023-12-06

    RAPIDPOINT 500e Blood Gas System Recalled Due to Drug Interference

    Siemens RAPIDPOINT 500e blood gas systems may show falsely elevated sodium readings in patients taking Perhexiline Maleate or Atomoxetine, risking misdiagnosis and inappropriate treatment of electrolyte imbalances.

    Product
    RAPIDPOINT 500e Blood Gas System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0471-2024·2023-12-06

    Breakfast sandwich recalled for undeclared milk and soy allergens

    Food Unlimited Breakfast Sandwich Bacon Egg & Cheddar Croissants are recalled due to undeclared milk and soy allergens. The affected products have Use By dates from 10/27/2023 to 11/8/2023.

    Product
    Breakfast Sandwich Bacon Egg & Cheddar Croissant Net Wt. 5.25oz (149g) UPC:766375253051. Packaged in clamshell container. Sold as single unit and 6 unit pack under Food Unlimited brand
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0411-2024·2023-12-06

    FloTrac Sensor Recalled Due to Potential Flushing Difficulties During Setup

    Edwards Lifesciences is recalling 1417 FloTrac Sensors used for intravascular pressure monitoring due to potential flushing difficulties during kit setup. No illnesses or injuries have been reported.

    Product
    FloTrac Sensor, REF: MHD8 & MHD85,MHD6R5, MHD8R, MHD8R5, MHD8S, STERILEEO, Rx only. For use in intravascular pressure monitoring.
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Devices)·Z-0409-2024·2023-12-06

    Acumen IQ Sensor Intravascular Pressure Monitor Flushing Difficulty

    Edwards Lifesciences is recalling 33,327 Acumen IQ Sensors used for intravascular pressure monitoring due to potential flushing difficulties during setup. The devices are distributed across the US and internationally.

    Product
    Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in intravascular pressure monitoring.
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Devices)·Z-0402-2024·2023-12-06

    Medical Device Screening Tool Recalled Due to Technical Distortion Issues

    PATH is recalling 28 units of SENTIERO Screening2 hearing examination devices due to potential technical distortions. The affected devices were distributed in Florida, Missouri, Ohio, and Wisconsin.

    Product
    SENTIERO Screening2, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S2
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0418-2024·2023-12-06

    Colonoscope Repair Defect May Cause Device Malfunction and Contamination Risk

    Aizu Olympus colonoscopes with improperly repaired light guide connectors may experience loss of image or suction failure. This could delay treatment and expose patients to contaminated material.

    Product
    PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE
    Category
    Medical Device
    Distribution
    6 states
  • SevereNHTSA·23V815000·2023-12-05

    Terberg Benschop Recalls Terminal Tractors for Steering Linkage Defect

    Terberg Benschop is recalling 2021-2022 YT193 terminal tractors because paint wear on the steering linkage may cause bolts to loosen or break, risking loss of steering control.

    Product
    TERBERG BENSCHOP B.V. — TERBERG BENSCHOP B.V. TERMINAL TRACTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V817000·2023-12-05

    Cushman Recalls 2024 Hauler Pro LSVs Due to Fire Risk

    Textron Specialized Vehicles is recalling 2024 Cushman Hauler Pro LSVs because water may enter the battery module, damaging circuits and increasing fire risk.

    Product
    CUSHMAN — CUSHMAN HAULER PRO LSV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24726·2023-12-05

    Foiresoft Zebra Roller Blinds Recalled for Strangulation Hazard

    Foiresoft Zebra Roller Blinds sold on Amazon.com have looped operating cords that pose a strangulation hazard to children. Consumers should stop using them immediately and contact Softfunch for a refund.

    Product
    Foiresoft Zebra Roller Blinds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V816000·2023-12-05

    Volvo 2024 VN and VHD: Incorrect Axle Weight Label Increases Overload Risk

    Certain 2024 Volvo VN and VHD trucks have an incorrect Gross Axle Weight Rating label, which can allow vehicles to be overloaded and increases crash risk. Dealers will replace the label free of charge.

    Product
    VOLVO — VOLVO VN, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V811000·2023-12-04

    Eldorado Axess and EZR Buses Recalled for Driveshaft Separation Risk

    Eldorado is recalling 2019-2023 Axess and EZR buses because a transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.

    Product
    ELDORADO — ELDORADO AXESS, EZR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V812000·2023-12-04

    Gillig Recalls 2021-2023 Low Floor Vehicles Due to Fire Risk

    Gillig is recalling 3,626 Low Floor vehicles from 2021-2023 because an incorrect fuse in the rearview mirror system may overheat and cause a fire.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V813000·2023-12-04

    Porsche Recalls 718 Models Due to Spoiler Visibility Issue

    Porsche is recalling certain 2023-2024 718 models because the rear spoiler may raise too high, reducing brake light visibility and increasing crash risk.

    Product
    PORSCHE — PORSCHE 718 BOXSTER S, 718 CAYMAN GTS, 718 BOXSTER GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V814000·2023-12-04

    2023 INFINITI QX60 Headlight System Malfunction Increases Crash Risk

    Nissan is recalling certain 2023-2024 INFINITI QX60 vehicles because the Adaptive Front-Light System may incorrectly adjust headlights downward at high speeds, reducing visibility and increasing crash risk.

    Product
    INFINITI — INFINITI QX60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V807000·2023-12-01

    Mercedes-Benz Recalls 2024 GLE 450e Due to Stopping Distance Issue

    Mercedes-Benz is recalling 2,797 2024 GLE 450e vehicles because a software error may increase the distance required to stop, raising crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450E 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·060-2023·2023-12-01

    Pelleh Poultry Recalls Ready-to-Eat Beef and Poultry Products for Listeria Risk

    Pelleh Poultry Corp. is recalling approximately 708 pounds of ready-to-eat beef and poultry products due to possible Listeria monocytogenes contamination.

    Product
    Pelleh Poultry Corp. — Pelleh Poultry Corp. Recalls Ready-To-Eat Beef and Poultry Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·23V808000·2023-12-01

    Spartan Fire Recalls 2020-2023 Fire Apparatus Due to Electrical Fire Risk

    Spartan Fire is recalling 69 fire apparatus units from 2020-2023 because a firmware defect may cause electrical circuits to overheat and start a fire.

    Product
    KME — KME, SPARTAN FIRE, SMEAL AERIAL FIRE APPARATUS, S-180 PUMPER, AERIAL, PUMPER FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide