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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27176–27200 of 90157

  • HighFDA (Devices)·Z-0508-2022·2022-01-26

    Cardinal Infant Heel Warmer recalled due to unapproved labeling changes

    Philips North America recalls Cardinal Infant Heel Warmers because labeling was changed without FDA approval. The devices cannot be sold or distributed without new FDA clearance.

    Product
    Cardinal Infant Heel Warmer, Reference # 989805617251 11470-010T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0502-2022·2022-01-26

    Blood Collection Tubes Recalled Due to Lithium Heparin Variation

    Greiner Bio-One is recalling 889,200 blood collection tubes (Lot #B21053QG) due to variation in lithium heparin that may cause blood clotting. The tubes were distributed to ten U.S. states.

    Product
    greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF 456087P
    Category
    Medical Device
    Distribution
    10 states
  • HighNHTSA·22V029000·2022-01-25

    Forest River Recalls Transit Buses Due to Fire Risk from Relay Module

    Forest River is recalling specific 2021-2023 transit buses because a failed relay module can increase the risk of a fire. Dealers will install a wire jumper harness free of charge.

    Product
    GLAVAL BUS — GLAVAL BUS, STARTRANS, STARCRAFT BUS COMMUTE, SENATOR II HD, ALLSTAR XLT, ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V030000·2022-01-25

    2021 Harley-Davidson Motorcycles Instrument Cluster May Fail in Cold Weather

    Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON RH1250S, RA1250S, RA1250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V031000·2022-01-25

    Kia Recalls Vehicles Due to Potential Air Bag Deactivation

    Kia is recalling specific 2017-2019 models because a defect may prevent air bags from deploying in a crash.

    Product
    KIA — KIA FORTE KOUP, SOUL EV, SEDONA, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V028000·2022-01-24

    Inland Empire Trailers Recalls 2021 Models Due to Axle Spindle Nut Issues

    Inland Empire Trailers is recalling 50 units of 2021 trailers because improperly tightened axle spindle nuts may cause overheating and loss of control.

    Product
    INLAND EMPIRE TRAILERS — INLAND EMPIRE TRAILERS UTILITY/ DUMP TRAILER, FLAT DECK TRAILER, ENCLOSED TRAILER, UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V027000·2022-01-24

    2022 Mitsubishi Outlander Recalled for Defective Fuel Pump

    Mitsubishi is recalling certain 2022 Outlander vehicles because the fuel pump may fail due to incorrectly fused internal components. Fuel pump failure can cause engine stall, increasing the risk of a crash.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V023000·2022-01-21

    BMW Recalls 2019-2020 K 1600 Motorcycles for Rear Suspension Defect

    BMW is recalling 2019-2020 K 1600 GT, GTL, and B motorcycles because a rear suspension link strut may be insufficiently strong, potentially affecting stability and increasing crash risk.

    Product
    BMW — BMW K 1600 GTL, K 1600 GT, K 1600 B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V025000·2022-01-21

    Rosenbauer Fire Trucks Recalled for Rear Axle Drive Pinion Fracture Risk

    Rosenbauer America is recalling 127 Commander, Warrior, and Avenger vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, WARRIOR, AVENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V022000·2022-01-21

    Kia Recalls 2020 Cadenza for Rear Power Window Safety Issue

    Kia is recalling 2020 Cadenza vehicles because rear power windows can operate after the ignition is off, increasing injury risk.

    Product
    KIA — KIA CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V026000·2022-01-21

    Trails West Recalls 2017-2021 Trailers Due to Propane Regulator Fire Risk

    Trails West is recalling 2017-2021 Sierra, Classic, Santa Fe, and Freeride trailers because a propane regulator may fail, increasing fire risk.

    Product
    TRAILS WEST — TRAILS WEST SIERRA, FREERIDE, CLASSIC, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E003000·2022-01-20

    Pacific Trailer Recalls RAM A Frame Couplers Due to Welding Defect

    Pacific Trailer is recalling RAM A Frame 2 5/16" couplers because improper welding may cause the trailer to separate from the tow vehicle.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V019000·2022-01-20

    Spartan Fire Vehicles Recalled for Rear Axle Drive Pinion Fracture Risk

    Marion Body Works is recalling 2021-2022 Spartan Fire vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning and increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V018000·2022-01-20

    2021-2022 Heartland RVs Recalled for Tire Belt Separation Risk

    Certain 2021-2022 Heartland Cyclone, Fuel, Gravity, and Road Warrior vehicles with Sailun tires may experience belt separation, risking loss of vehicle control. Dealers will replace affected tires at no cost.

    Product
    HEARTLAND — HEARTLAND CYCLONE, GRAVITY, FUEL, ROAD WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0366-2022·2022-01-19

    Howling Cow Butter Almond Ice Cream recalled for undeclared allergens

    Howling Cow Butter Almond ice cream sold in North Carolina and South Carolina contains Cookie Dough Ice Cream with undeclared soy and wheat allergens. Consumers with allergies should not consume the product.

    Product
    butter almond HOWLING COW THE ICE CREAM OF NC STATE UNIVERSITY One Pint (473 ml) Ingredients: Milk, Cream, Sugar, Almonds***Stabilizer***Carmel Color and Natural Flavor. Contains milk, almonds Proudly distributed by Hunter Farms High Point, NC 27262 UPC 0 74336 65079 6
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0494-2022·2022-01-19

    Ultimate Performance Labs Flexable Capsules recalled for undeclared shellfish

    NutraCap Labs LLC is recalling Ultimate Performance Labs Flexable Capsules 90ct Bottles due to undeclared shellfish content. Consumers with shellfish allergies face risk of allergic reaction.

    Product
    Ultimate Performance Labs Flexable Capsules 90ct Bottles UPC CODE 1 95893 4707 8
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0403-2022·2022-01-19

    Adrenalyne Crimson Crush Fruit Punch Recalled for Undeclared Shellfish

    NutraCap Labs LLC is recalling Adrenalyne Crimson Crush Fruit Punch 25oz jars because they contain undeclared shellfish. The recall affects 80,169 units distributed across 25 states.

    Product
    Adrenalyne Crimson Crush Fruit Punch 25oz jar
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0431-2022·2022-01-19

    Dynamik Muscle Warbringer Capsules recalled for undeclared milk

    NutraCap Labs is recalling Dynamik Muscle Warbringer Capsules because the product contains undeclared milk, which poses a risk to consumers with milk allergies.

    Product
    Dynamik Muscle Warbringer Capsules 90ct Bottle UPC CODE 5 00102 92106
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0433-2022·2022-01-19

    Enduring Atlas Keto Sleep Capsules Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Enduring Atlas Keto Sleep Capsules (120ct, UPC X001V3J6ZL, Lot #2012314, Exp 12/2022) because the product contains undeclared milk, posing a risk to consumers with milk allergies.

    Product
    Enduring Atlas Keto Sleep Capsules 120ct Bottle UPC CODE X001V3J6ZL
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0461-2022·2022-01-19

    MB Nutrition Sleep + Capsules Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling MB Nutrition Sleep + Capsules (60ct, UPC 860005918201) because the product contains undeclared milk, a major allergen. The product was distributed across 25 U.S. states.

    Product
    MB Nutrition Sleep + Capsules 60ct Bottle UPC CODE 8 60005 91820 1
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0436-2022·2022-01-19

    Fit Farm USA Z-Burn Sleep Smart Capsules Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Fit Farm USA Z-Burn Sleep Smart Capsules 60ct bottles because they contain undeclared milk. The product was distributed across 25 states.

    Product
    Fit Farm USA Z-Burn Sleep Smart Capsules 60ct Bottle UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0455-2022·2022-01-19

    Liquid Lucky Kiwi Lime Sample Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Liquid Luck Liquid Lucky Kiwi Lime Sample bottles and jars because they contain undeclared milk, a major allergen. The product was distributed across 25 US states.

    Product
    Liquid Luck Liquid Lucky Kiwi Lime Sample NO UPC CODE
    Category
    Food
    Distribution
    26 states