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.

19201–19225 of 50410

  • HighNHTSA·21V755000·2021-09-28

    2022 Thor Motor Coach Rize Motorhomes Recalled for LP Gas Line Rupture Risk

    Thor Motor Coach is recalling 2022 Rize and Scope motorhomes due to an LP gas line that may be too short and improperly installed. A gas leak from a ruptured line could cause a fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH RIZE, SCOPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V767000·2021-09-28

    Entegra Class A Motorhomes Recalled for Fuel Hose Leak Fire Risk

    Entegra Coach is recalling certain 2021-2022 Anthem, Aspire, and Reatta XL Class A motorhomes with Cummins diesel engines due to fuel hoses that may leak and pose a fire risk. Owners should contact Entegra customer service at 1-800-283-8267 for free replacement.

    Product
    ENTEGRA — ENTEGRA ANTHEM, REATTA XL, ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V754000·2021-09-28

    Thor Motor Coach Omni motorhomes recalled for LP gas line fire hazard

    Thor Motor Coach is recalling 2021-2022 Omni and Magnitude motorhomes due to an LP gas line routing defect. The line may be incorrectly routed through the rear suspension leaf springs, potentially causing a gas leak and fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH redundant MAGNITUDE, OMNI, MAGNITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V757000·2021-09-28

    Rosenbauer Recalls Fire Trucks Due to Improperly Crimped Lifting Cables

    Rosenbauer America is recalling specific 2020-2022 fire trucks because improperly crimped lifting cables may detach, causing the generator set to fall and increasing injury risk.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL HV507, PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V756000·2021-09-28

    Thor Motor Coach Recalls 2021-2022 Venetian Motorhomes for Awning Defect

    Thor Motor Coach is recalling 2021-2022 Venetian motorhomes because improperly installed patio awnings may separate while driving, increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH VENETIAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V750000·2021-09-27

    2020-2021 Mazda CX-9 second-row seat may slide forward in crash

    Mazda is recalling certain 2020-2021 CX-9 vehicles with 60/40 split bench second-row seats. The left-side second-row seat may unexpectedly slide forward during a crash, increasing injury risk to occupants.

    Product
    MAZDA — MAZDA CX-9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V749000·2021-09-24

    Hyundai Recalls Sonata Models for Turn Signal Software Defect

    Hyundai is recalling 2015-2017 Sonata models because a software defect may cause turn signals to activate in the opposite direction, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI SONATA, SONATA HYBRID, SONATA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V745000·2021-09-24

    Fifth Wheel Trailers Recalled for Incorrect Weight Rating Placard

    Forest River Wildwood and Salem fifth wheel trailers from 2021-2022 are recalled due to incorrect Gross Vehicle Weight Rating (GVWR) listed on the Federal Placard. An overloaded pin box can fail, increasing the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V741000·2021-09-23

    Daimler Recalls 2015-2018 Thomas Built Minotour School Buses for Fire Risk

    Daimler Trucks North America is recalling 2015-2018 Thomas Built Minotour school buses because a corroded solenoid connector may cause an electrical short, leading to fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V743000·2021-09-23

    2022 Nissan Pathfinder Seat Frame Welds May Fail in Crash

    Nissan is recalling certain 2022 Pathfinder vehicles because the second-row seat back frames may have insufficient welds that could separate. This could cause seats to fail to restrain occupants properly during a crash, increasing injury risk.

    Product
    NISSAN — NISSAN PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·032-2021·2021-09-23

    Ready Pac Foods Recalls Salads with Undeclared Anchovy Allergen

    Ready Pac Foods is recalling ready-to-eat salads containing meat and poultry because they include salad dressing with an undeclared anchovy allergen.

    Product
    Ready Pac Foods, Inc. Recalls Ready to Eat Salad Products Containing Meat and Poultry Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V739000·2021-09-23

    2021 Chevrolet Tahoe Fuel Pump Module Recall for Engine Stall Risk

    General Motors is recalling certain 2021 Chevrolet Tahoe vehicles due to a fuel pump power control module defect that may cause engine stalls, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE ESV, ESCALADE, SUBURBAN, ESCALADE NA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V737000·2021-09-23

    MCI Motorcoaches Recalled for Wheelchair Lift Barrier Failure Risk

    Motor Coach Industries is recalling 2005-2012 MCI J4500 and E4500 motorcoaches because the wheelchair lift's outer barrier may fail under force, increasing injury risk.

    Product
    MCI — MCI J4500, E4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V738000·2021-09-23

    Ducati Recalls 2019 Hypermotard 950 SP for Side Stand Welding Defect

    Ducati is recalling 2019 Hypermotard 950 SP motorcycles because the side stand may be improperly welded. A broken stand could cause the motorcycle to fall, increasing injury risk.

    Product
    DUCATI — DUCATI HYPERMOTARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21784·2021-09-23

    Polaris Phoenix 200 ATVs Recalled for Crash Hazard

    Polaris is recalling about 13,000 model year 2011–2021 Phoenix 200 ATVs because the throttle speed control stop can break and become stuck, posing a crash hazard. The company has received 18 reports of throttle stop failure including one crash with minor injury.

    Product
    Model Year 2011-2021 Phoenix 200 ATV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0976-2021·2021-09-22

    Vita Aid Keto-Elemental Nutrition Powder Recall: Undeclared Milk

    Naturo Aid Pharmaceutical Inc. is recalling Vita Aid Keto-Elemental Nutrition (Chocolate) powder due to undeclared milk contamination. The product may pose a risk to consumers with milk allergies.

    Product
    Vita Aid Keto-Elemental Nutrition (Chocolate), VA-958. The product is a powder, packaged in an aluminum bag , with a net weight of 315g.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2444-2021·2021-09-22

    Roche cobas infinity software may release incorrect test results to laboratories

    Roche Diagnostics is recalling cobas infinity central lab software versions 3.01.03–3.02.08 because under certain circumstances, the software may automatically send false test results to laboratory information systems. Correct results remain available on the instrument.

    Product
    cobas infinity central lab running software version 3.01.03 through 3.02.08, Catalog#: 07154003001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0969-2021·2021-09-22

    Full Tilt Thai Tea Ice Cream Recall for Insufficient Pasteurization

    Full Tilt Ice Cream is recalling Thai Tea ice cream in 16oz pints and 3-gallon tubs because the ice cream mix did not meet pasteurization specifications, creating a risk of harmful bacterial contamination.

    Product
    Thai Tea, Full Tilt Ice Cream brand, packaged in 16oz pre packed pints and 3 gallon tubs. UPC on pint container: 00856962005290.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2467-2021·2021-09-22

    BD SmartSite Needle-Free Connector Valves Recalled for Flow and Occlusion Issues

    CAREFUSION is recalling BD SmartSite needle-free connector valves due to difficulty flushing, flow issues, and occlusions that could delay therapy. Approximately 23.8 million units were distributed worldwide.

    Product
    BD SmartSite, REF: 2000E CHINA; BD SmartSite Connector, REF: 2000E-04; BD SmartSite J-LOOP Extension Set One Needle Free Valve, REF: 20021E7D; BD SmartSite Extension Set One Needle Free Valve Slip Luer, REF: 20037E7D; BD SmartSite Extension Set 3 Needle Free Valves, REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2457-2021·2021-09-22

    BD Syringe Set Needle-Free Connector Valves May Cause Therapy Delay

    BD Syringe Set needle-free connector valves may experience difficulty flushing, flow issues, or occlusions that could delay patient therapy. About 16,700 units have been distributed worldwide.

    Product
    BD Syringe Set 20 DP MIC TBG 0.2MF CKV Anti-Siphon SmartSite VLV Sensing Disc, REF: 10798696; BD Syringe Set 20 DP MIC TBG CKV Anti-Siphon SmartSite VLV Sensing Disc, REF: 10798703;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21199·2021-09-22

    Oceanic Adult Dry Top Snorkels Recalled Due to Drowning Hazard

    Huish Outdoors is recalling Oceanic Adult Dry Top Snorkels sold at Costco because the bottom purge valve can leak, allowing unexpected water entry that poses a drowning hazard. Consumers should stop using the snorkels immediately.

    Product
    Oceanic Adult Dry Top Snorkels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2450-2021·2021-09-22

    Diagnostic reagent kits recalled for incorrect chemical composition

    Gibson Bioscience is recalling Potassium Hydroxide 10% diagnostic reagent kits (Lot 21137116, 11 units) manufactured with Hydrogen Peroxide 3% instead of the intended chemical. The wrong solution could cause inaccurate laboratory test results.

    Product
    Potassium Hydroxide 10% (KOH 10%), Cat. No. 300145 Potassium Hydroxide 10% (KOH 10%) is intended for use in the demonstration of yeast and fungal elements in wet clinical preparations. Potassium Hydroxide digests the proteinaceous material in the specimen, leaving the fungal…
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Food)·F-0982-2021·2021-09-22

    Jimbo's Bloody Mary Mix Recalled for Undeclared Soy, Sulfites, Wheat

    Jimbo's Kitchen is recalling Jimbo's Bloody Mary Mix because the product contains soy, sulfites, and wheat that are not declared on the ingredient label, posing a risk to consumers with allergies or sensitivities.

    Product
    Jimbo's BLOODY MARY MIX; 2.5OZ MAKES ABOUT 45 SERVINGS; Ingredients: Horseradish Powder, Parsley, Worcestershire Powder, Cayenne Pepper, Lemon Peel, Black Pepper, Celery Seed Powder, Lemon Juice Crystals, Sea Salt; Hand made in a facility that contains wheat, dairy, eggs and…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2455-2021·2021-09-22

    BD SmartSite Needle-Free Valve Extension Set Recalled for Potential Occlusion

    CareFusion recalls BD SmartSite needle-free valve extension sets due to potential occlusion, flow issues, and difficulty flushing that could delay medical therapy.

    Product
    BD SmartSite 'Y' Extension Set 2 Needle-Free Valves, REF: 20019E7D
    Category
    Medical Device
    Distribution
    Distributed nationwide