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.

20476–20500 of 50413

  • HighNHTSA·21V348000·2021-05-13

    Prevost Recalls 2021 X3 Commuter Coaches Due to Seat Belt Assembly Defect

    Prevost is recalling 2021 X3 Commuter Coaches because incorrectly assembled seat belts at flip-up seats may sit improperly on wheelchair users, increasing injury risk.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21747·2021-05-13

    Leisure Time Recalls Brutus Swing Sets Due to Injury Hazard

    Leisure Time Products is recalling about 9,000 Brutus metal swing sets because the swing hanger attachment can fail, causing the swing to fall.

    Product
    Backyard Discovery Big Brutus, Little Brutus and Mini Brutus metal A-frame swing sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21745·2021-05-13

    The Lye Guy Recalls Sodium and Potassium Hydroxide for Packaging Defects

    The Lye Guy is recalling sodium and potassium hydroxide products because the packaging is not child-resistant and labels violate federal hazardous substance requirements.

    Product
    The Lye Guy Sodium Hydroxide and Potassium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21744·2021-05-13

    Polaris Recalls 2021 RZR PRO XP Vehicles Due to Fire Hazard

    Polaris is recalling about 32 Model Year 2021 RZR PRO XP and RZR PRO XP 4 off-road vehicles because a missing copper seal washer can cause an oil leak and fire hazard.

    Product
    Model Year 2021 RZR PRO XP and RZR PRO XP 4 (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21743·2021-05-13

    Alliance Chemical Recalls Sodium Hydroxide Products for Packaging and Labeling Violations

    Alliance Chemical is recalling sodium hydroxide products because the packaging is not child-resistant and labels violate federal hazardous substance laws.

    Product
    Sodium Hydroxide Flakes, Pure Lye, Caustic Soda Drain Cleaner and Sodium Hydroxide Flake (Caustic Soda Flake)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V346000·2021-05-13

    GM Recalls 2019 Chevrolet 6500HD Trucks for Engine Software Defect

    General Motors is recalling 2019 Chevrolet 6500HD trucks because an engine software error allows speeds exceeding the tires' maximum rating, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET SILVERADO 6500, 6500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0480-2021·2021-05-12

    Hostess SnoBalls Recalled for Undeclared Coconut Allergen

    Hostess Brands is recalling SnoBalls snack cakes packaged with Chocolate CupCakes labels because the packaging fails to declare the major food allergen coconut.

    Product
    Hostesss SnoBalls packaged as Hostess Chocolate CupCakes, Net Wt 3.17 OZ, UPC 8 88109 01001 0, Hostess Brands, LLC Kansas City, MO
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-1534-2021·2021-05-12

    Greiner Bio-One Recalls VACUETTE Blood Collection Tubes for Insufficient Draw Volume

    Greiner Bio-One is recalling VACUETTE blood collection tubes because insufficient draw volume may cause erroneous coagulation test results.

    Product
    VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged - Product Usage: indicated for use in collection and transport of venous whole blood for coagulation testing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1522-2021·2021-05-12

    Medtronic Recalls CareLink SmartSync Device Manager Due to Software Error

    Medtronic is recalling 16,311 CareLink SmartSync Device Managers because a software issue may overestimate the remaining battery life of implanted cardiac devices.

    Product
    CareLink SmartSync Device Manager (24970A). used to interrogate cardiac implantable electronic devices (CIED).
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1533-2021·2021-05-12

    GE Healthcare Recalls Centricity Universal Viewer for Patient Data Mismatch Risk

    GE Healthcare is recalling 112 units of Centricity Universal Viewer software because a specific configuration may display comparison exams from the wrong patient.

    Product
    Centricity Universal Viewer - Product Usage: intended to assist in the viewing, analysis, diagnostic interpretation, and sharing of images and other information.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V341000·2021-05-12

    2021 Porsche Cayenne GTS Engine Cylinder Bore Crack Recall

    Porsche is recalling 2021 Cayenne GTS vehicles due to engine cylinder bore cracks that may cause engine damage, stalling, or oil leaks, increasing the risk of a crash or fire. Dealers will replace the engine at no charge.

    Product
    PORSCHE — PORSCHE CAYENNE GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0475-2021·2021-05-12

    REDCON1 Recalls MRE LITE Protein Powder for Undeclared Wheat and Soy

    REDCON1 LLC is recalling MRE LITE Animal Based Protein powder because it contains undeclared wheat and soy allergens.

    Product
    MRE LITE Animal Based Protein, Oatmeal Chocolate Chip, Animal Protein Powder Drink Mix, Net Wt. 30.69 oz (1.92lb) (870g)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1523-2021·2021-05-12

    Medtronic Recalls CRT-P Quad Models Due to Software Longevity Error

    Medtronic is recalling 45,411 CRT-P Quad implantable devices worldwide because a software issue overestimates battery longevity for six months before replacement is due.

    Product
    CRT-P Quad Models (CRT-Ps): a. Percepta CRT-P MRI: W1TR01, W1TR04, W4TR01, W4TR04 b. Serena CRT-P MRI: W1TR02, W1TR05, W4TR02, W4TR05 c. Solara CRT-P MRI: W1TR03, W1TR06, W4TR03, W4TR06. implantable medical devices used to treat arrhythmias related to bradycardia, and…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1535-2021·2021-05-12

    Medtronic Intellis Recharger Recalled for Potential Unintended Heating

    Medtronic is recalling 79,616 Intellis Model 97755 Rechargers worldwide due to a potential for unintended heating.

    Product
    Intellis Model 97755 Recharger - Product Usage: designed to charge the following Medtronic rechargeable neurostimulators:  Intellis with AdaptiveStim Technology Model 97715 Implanted Neurostimulator  Intellis Model 97716 Implanted Neurostimulator.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·21V343000·2021-05-12

    2021 Gulf Stream Travel Trailers Recalled for Incorrect Tire Pressure Labels

    Gulf Stream is recalling certain 2021 travel trailers because the Federal Certification Label lists incorrect tire size and pressure information. Overinflated tires increase the risk of crashes.

    Product
    GULF STREAM — GULF STREAM VINTAGE CRUISER, GEO, NORTHERN EXPRESS, MATRIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21133·2021-05-12

    Briggs & Stratton Recalls Log Splitters Due to Engine Kickback Injury Hazard

    Briggs & Stratton is recalling YTL, Longli, and TIYA log splitters with 250cc engines due to a kickback hazard that caused two broken wrists.

    Product
    YTL, Longli and TIYA Log Splitters with Briggs & Stratton® 250cc engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V344000·2021-05-12

    2021 Airstream Interstate Nineteen bus bar electrical fire hazard

    Airstream is recalling certain 2021 Interstate Nineteen motorhomes due to potentially incorrectly wired bus bar circuit breakers that may overheat and create a fire risk. Dealers will relabel and relocate the affected wires free of charge.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE NINETEEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0491-2021·2021-05-12

    JKH Enterprises Recalls Peanut Brittle for Milk Allergen Mislabeling

    JKH Enterprises is recalling 30 packages of Granny's Fudge Gorgeous Peanut Brittle because the label declares unsalted cream but fails to list milk as an ingredient.

    Product
    Granny's Fudge Gorgeous Peanut Brittle, net wt. 5oz. or 8 oz, packed in a clear plastic container. No UPC. Label declares "***Ingredients: Sugar, peanuts, corn syrup, butter, vanilla, baking soda***Allergy Information: Mfg on same equipment that processes wheat, egg, peanut…
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V345000·2021-05-12

    2020-2021 Airstream Travel Trailers Recalled for Fire Risk from Incorrectly Installed Stove

    Airstream is recalling certain 2020 and 2021 Flying Cloud and International travel trailers because the stove was incorrectly installed in a non-sealed cabinet. Drafts can force flames into the cabinet, creating a fire hazard.

    Product
    AIRSTREAM — AIRSTREAM INTERNATIONAL, FLYING CLOUD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1526-2021·2021-05-12

    Medtronic Recalls CRT-P Pacemakers Due to Longevity Estimation Error

    Medtronic is recalling specific implantable cardiac resynchronization therapy pacemakers because a longevity estimation error may occur in the early years of device life.

    Product
    Implantable cardiac resynchronization therapy pacemakers (CRT-P) - Product Usage: used to treat arrhythmias related to bradycardia. Additionally, CRT-P devices can also provide cardiac resynchronization therapy (CRT) in treatment of heart failure. 1. Percepta family: Percepta…
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·21V334000·2021-05-11

    Rosenbauer Fire Trucks Recalled for Fuel Rail Leak Fire Risk

    Rosenbauer America is recalling 2016-2021 fire trucks because a fuel rail leak could cause a fire. Owners should contact the dealer for a free repair.

    Product
    ROSENBAUER — ROSENBAUER WARRIOR, AVENGER, COMMANDER, COMMERCIAL M2-106
    Category
    Vehicle
    Distribution
    Distributed nationwide