The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

17801–17825 of 50404

  • HighNHTSA·22V173000·2022-03-22

    Hi-Tech E.V.S. Recalls Spartan Emergency Vehicles for Display Defect

    Hi-Tech E.V.S. is recalling 2020 Spartan MetroStar and 2021 Spartan Gladiator emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    HI-TECH E.V.S. — HI-TECH E.V.S. SPARTAN METROSTAR, SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V170000·2022-03-21

    2022 Heartland Travel Trailers Recalled for Electrical Fire Risk

    Heartland is recalling certain 2022 Trail Runner, Prowler, and Lithium travel trailers with defective power inlet bolts that may loosen, creating an electrical fire hazard. Dealers will inspect and replace the inlet free of charge.

    Product
    HEARTLAND — HEARTLAND PROWLER, LITHIUM, TRAIL RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E021000·2022-03-18

    Dometic Recalls 2-Burner Cooktops Due to Gas Leak Risk

    Dometic is recalling specific 2-burner cooktops because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V167000·2022-03-18

    Mercedes-Benz Recalls S-Class and EQS Models for Turn Signal Software Error

    Mercedes-Benz is recalling 2021 S 500/S 580 and 2022 EQS 450/580 vehicles because a software error may disable rear turn signals, hazard lights, and reverse lights.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 500, EQS 580, EQS 450, S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V169000·2022-03-18

    Tesla Recalls Model 3, S, and X for Rearview Camera Delay

    Tesla is recalling certain Model 3, S, and X vehicles because the rearview camera image may not display immediately when reversing, increasing crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V164000·2022-03-17

    International LT vehicles recalled for battery cable fire risk

    Navistar is recalling 2018-2023 International LT vehicles with 1500W Purkeys inverter systems. The positive battery cable may be incorrectly routed, causing it to chafe and become damaged, which increases the risk of electrical fire.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V165000·2022-03-17

    GM Recalls 2014-2015 Chevrolet Equinox and GMC Terrain for Wiper Defect

    General Motors is recalling 2014-2015 Chevrolet Equinox and GMC Terrain vehicles because corroded ball joints may cause windshield wipers to fail, reducing visibility.

    Product
    GMC — GMC, CHEVROLET TERRAIN, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22733·2022-03-17

    Acme United Recalls PhysiciansCare Over-the-Counter Drugs for Non-Compliant Packaging

    Acme United is recalling PhysiciansCare brand over-the-counter pain relievers and aspirin because the packaging is not child-resistant as required by law, creating a poisoning risk for young children.

    Product
    PhysiciansCare brand Aspirin, Extra Strength Non Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0850-2022·2022-03-16

    Strawberry Coffee Cake Recalled for Undeclared Egg, Milk, and Wheat Allergens

    Chicago Sweet Connections is recalling its Strawberry Flavor Coffee Cake due to undeclared allergens: egg, milk, and wheat. Consumers with allergies to these ingredients should not consume the product.

    Product
    Chicago Sweet Connections: Coffee Cake - Strawberry Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0844-2022·2022-03-16

    Chicago Sweet Connections Coffee Cake Recalled for Undeclared Allergens

    Chicago Sweet Connections is recalling its Coffee Cake - Cheese Flavor due to undeclared allergens: egg, milk, and wheat. The product was distributed to retail locations in Illinois and Wisconsin.

    Product
    Chicago Sweet Connections: Coffee Cake - Cheese Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0849-2022·2022-03-16

    Chicago Sweet Connections Coffee Cake Contains Undeclared Egg, Milk, and Wheat Allergens

    Chicago Sweet Connections is recalling its Coffee Cake - Raspberry Flavor because it contains undeclared egg, milk, and wheat allergens that are not listed on the product label.

    Product
    Chicago Sweet Connections: Coffee Cake - Raspberry Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0851-2022·2022-03-16

    Del Monte Bubble Fruit cups recalled for potential metal fragments

    DEL MONTE FOODS INC is recalling Del Monte Bubble Fruit Tropical Mixed Fruit Cup Snacks due to potential metal fragments approximately 2–3 mm in size. No injuries have been reported.

    Product
    Del Monte Bubble Fruit - Tropical Mixed Fruit Cup Snacks. Mixed fruit and popping boba with sweetened juice. 3.5 0z (4 pack), 6 x 4 pack sleeves per carton UPC: 24000 25236
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0847-2022·2022-03-16

    Coffee Cake with Undeclared Egg, Milk, and Wheat Allergens

    Chicago Sweet Connections is recalling Coffee Cake - Custard Flavor due to undeclared allergens: egg, milk, and wheat. Consumers with allergies to these ingredients should not consume the product.

    Product
    Chicago Sweet Connections: Coffee Cake - Custard Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0829-2022·2022-03-16

    Factor 75 Chili Meal Recalled for Undeclared Milk Allergen

    Factor 75 Fiery Beef & Black Bean Chili meals are being recalled due to undeclared milk allergen. The product was distributed nationwide and may affect consumers with milk allergies.

    Product
    Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·F-0843-2022·2022-03-16

    Chicago Sweet Connections Coffee Cake Recalled for Undeclared Egg, Milk, and Wheat Allergens

    Chicago Sweet Connections coffee cake may contain undeclared egg, milk, and wheat allergens. The product was distributed to retail locations in Illinois and Wisconsin.

    Product
    Chicago Sweet Connections: Coffee Cake - Blueberry Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0733-2022·2022-03-16

    ExacTrac Dynamic Software Yaw Angle Error May Affect Radiotherapy Positioning

    ExacTrac Dynamic radiotherapy positioning software (versions 1.0.0–1.0.3) may calculate incorrect yaw angle for patient positioning with Varian linear accelerators, potentially affecting cone-beam CT imaging setup accuracy during radiotherapy.

    Product
    ExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. 1.0.0 INST; 20910-01A, ETD Positioning and Moni. 1.0.1 INST; 20910-01B, ETD Positioning and Moni. 1.0.2 INST; and 20910-01C ETD Positioning and Moni. 1.0.3 INST.
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Food)·F-0825-2022·2022-03-16

    LUPAG Dried Salted Plums Recalled for Elevated Lead Levels

    LUPAG brand Plain Dried Salted Plums are being recalled by Rojas Inc. due to elevated lead levels. Consumers should not eat this product.

    Product
    LUPAG brand Plain Dried Salted Plums, net wt. 0.5oz, pre-priced at $.99 packaged in transparent poly bags sealed with a cardboard header, stapled one dozen packages on a cardboard strip. UPC 7 25535 01133 7. Ingredients: Dried Prunes, salt. Origin: Taiwan or China Rojas…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0820-2022·2022-03-16

    Pineapple Rum Cake Recalled for Undeclared Allergens: Eggs, Wheat, Milk

    Edible Spirits, Inc. is recalling Pineapple Rum Cake because the product labels fail to declare eggs, wheat, and milk. Consumers with allergies to these ingredients should not consume this product.

    Product
    Pineapple Rum Cake
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0747-2022·2022-03-16

    Proton Therapy Systems May Fail to Verify Beam Range After Pause

    Proton therapy systems from Ion Beam Applications may not verify that beam range settings remain unchanged after treatment pause, risking incorrect treatment delivery if the range was manually modified.

    Product
    ProteusPLUS and ProteusONE- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation Proteus 235
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Food)·F-0834-2022·2022-03-16

    Chicago Sweet Connections Paczkis Recalled Due to Undeclared Allergens

    Chicago Sweet Connections is recalling Cheese Flavor Paczkis due to undeclared allergens: egg, milk, and wheat. The product was distributed to retail locations in Illinois and Wisconsin.

    Product
    Chicago Sweet Connections: Paczkis - Cheese Flavor packaged in a clear plastic clamshell 4 pack
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·22V163000·2022-03-16

    2022 Volkswagen Golf R engine design cover fire risk recall

    The engine design cover in 2022 Volkswagen Golf R vehicles may loosen during high acceleration and contact hot engine surfaces, increasing fire risk. Dealers will remove it free of charge.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF R, GTI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0741-2022·2022-03-16

    FISH Diagnostic Probe Kit Color Labeling Error Affects Test Results

    Cytocell Ltd. is recalling a Del(5q) Deletion FISH Probe Kit due to incorrect color labeling on probe components. The mislabeling may cause misinterpretation of test results for patients with AML or MDS.

    Product
    Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LPH024
    Category
    Medical Device
    Distribution
    Distributed nationwide