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.

19951–19975 of 50413

  • HighFDA (Food)·F-0754-2021·2021-07-07

    URBAN MEADOW Dry Roasted Unsalted Peanuts Recalled for Aflatoxin

    The Leavitt Corporation is recalling URBAN MEADOW brand dry roasted unsalted peanuts (16 oz jars) because the product may contain high levels of aflatoxin, a naturally occurring toxin that can cause serious health effects.

    Product
    URBAN MEADOW brand DRY ROASTED UNSALTED PEANUTS; NET WT 16OZ; INGREDIENTS: DRY ROASTED PEANUTS
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1989-2021·2021-07-07

    Philips Medical Monitor Bracket May Detach from Ceiling Mount

    Philips medical imaging monitors with worn bracket assembly shafts may detach from ceiling suspensions and fall on patients, operators, or staff. No injuries have been reported.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 882476 - Gemini TF Big Bore PET/CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0746-2021·2021-07-07

    JUST Egg Plant-Based Bites Recalled for Undeclared Egg and Milk

    Cuisine Solutions is recalling JUST Egg Inspired by Japan Portobello plant-based egg bites because they contain undeclared egg and milk. Consumers with allergies or sensitivities to these allergens should not consume the product.

    Product
    JUST Egg Inspired by Japan Portobello, Mushrooms, Sweet Potatos, Furikake, Soy 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402523, Expiration dates 3/5/2022, 3/31/2022, and 4/9/2022.16 cartons per corrugated case, Carton GTIN 7 05044 02523 0, Case Bar Code 10 750…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1970-2021·2021-07-07

    SNS Disposable Urethral Catheter Electrode Recalled for Sterilization Process Deviations

    Spes Medica has recalled SNS Disposable Urethral Catheter Electrodes due to possible deviations in ethylene oxide sterilization processes. The recall affects one lot distributed in California, Massachusetts, and South Carolina.

    Product
    SNS Disposable Urethral Catheter Electrode, 14 Fr, Gold Recording/Stimulating Contact printed on polyurethane film adhesive with attached 2 meter lead-wire with touch-proof connector, Reference Number UE002
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-1963-2021·2021-07-07

    Edwards VAMP Jr. blood management system pressure tubing may detach

    Edwards Lifesciences is recalling 1,679 units of Edwards VAMP Jr. 6 in blood management systems (lot 63445142, 63630816) due to potential pressure tubing detachment.

    Product
    Edwards VAMP Jr. 6 in (15 cm) REF: VMP306, Blood Management System, Rx Only, Single Use, CE, Sterile EO UDI: (01)57460691944782
    Category
    Medical Device
    Distribution
    33 states
  • HighFDA (Devices)·Z-1981-2021·2021-07-07

    Monitor bracket assembly recalled for detachment hazard on CT imaging systems

    Philips is recalling 1,301 monitor bracket assemblies for CT/PET-CT imaging systems due to shaft wear that could cause detachment from the suspension arm, potentially resulting in the monitor falling and serious injury.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT systems. Brilliance 16 Power, Brilliance 16/10/6 Water/Air 728240/728245/728246 - Brilliance 16 728255/728256/728266 - Brilliance 6 728250/728251…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0743-2021·2021-07-07

    JUST Egg Sous Vide Plant Egg Bites recalled for undeclared egg and milk

    Cuisine Solutions is recalling JUST Egg Inspired by America Roasted Potato, Dill, Chives, Red Bell Pepper, Black Pepper Sous Vide Plant Egg Bites because the product contains undeclared egg and milk allergens that are not listed on the label.

    Product
    JUST Egg Inspired by America Roasted Potato, Dill, Chives, Red Bell Pepper, Black Pepper 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402503, Expiration dates 2/22/2022, 3/1/2022, 3/8/2022, 2/22/2022, and 4/6/2022. 16 cartons per corrugated case, Carton GTIN 7 05044…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1966-2021·2021-07-07

    Edwards TruWave Pressure Monitoring Set Recalled Due to Tubing Detachment Risk

    Edwards Lifesciences is recalling Edwards TruWave (3 cc)/VAMP Jr Pressure Monitoring Sets (Lot 63545959) due to a potential risk that pressure tubing may detach from the blood sampling system.

    Product
    Edwards TruWave (3 cc)/VAMP Jr, REF: VMP406PX, Pressure Monitoring Set, Rx Only, CE UDI: (01)07460691958746
    Category
    Medical Device
    Distribution
    33 states
  • HighFDA (Devices)·Z-1991-2021·2021-07-07

    PowerPICC Catheter Kits Recalled for Incorrect Micro-Introducer Components

    Bard Access Systems is recalling 180 units of 5Fr PowerPICC Catheter kits because they contain incorrect micro-introducers.

    Product
    5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology PiCC with Microintroducer
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-1980-2021·2021-07-07

    Philips Continuous CT Fluoroscopy Monitor Bracket Assembly Fall Risk

    Philips is recalling 1,301 Monitor Bracket Assemblies due to shaft wear that could cause the assembly to detach from the ceiling suspension arm. This could result in the monitor falling and causing serious injury to patients, operators, bystanders, or service personnel.

    Product
    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and MX16 Models: 728131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21E061000·2021-07-06

    Yorkim LED Headlight Bulbs Recalled for Excessive Glare and Brightness

    Guangzhou Yorkim Trading Co., Ltd is recalling Yorkim R7 H11 LED bulbs sold on Amazon because they create excessive glare, failing federal safety standards.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V506000·2021-07-02

    Newmar recreational vehicles recalled for fuel rail sealing defect

    Newmar recalls 2017-2021 Mountain Aire, New Aire, Ventana, and Dutch Star RVs with Cummins diesel engines for a fuel rail sealing defect that can leak, increasing fire risk. Owners should contact Newmar for free inspection and repair.

    Product
    NEWMAR — NEWMAR NEW AIRE, VENTANA, DUTCH STAR, MOUNTAIN AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V508000·2021-07-02

    2020-2021 Braxton Creek Travel Trailers Recalled for Stove Gas Leak Risk

    Braxton Creek is recalling 2020 and 2021 LX and BX travel trailers with Dometic cooking stoves due to an overtightened saddle valve bolt that can damage the o-ring seal and cause a continuous gas leak, posing a fire risk.

    Product
    BRAXTON CREEK — BRAXTON CREEK LX, BX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V509000·2021-07-02

    Mercedes-Benz Recalls Vehicles for Incorrectly Adjusted LED Headlights

    Mercedes-Benz is recalling specific 2018-2021 models because LED headlights may have been incorrectly adjusted during repair, reducing visibility and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, AMG GLE63, GLE 580, AMG GLE53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V500000·2021-07-01

    Jaguar Recalls 2018 F-Type for Front Passenger Air Bag Defect

    Jaguar is recalling one 2018 F-Type vehicle because the instrument panel may interfere with the front passenger air bag, potentially causing it to tear during deployment.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V494000·2021-07-01

    Mazda Recalls 2004-2007 Mazda3 for Air Bag Cover Shattering Risk

    Mazda is recalling 2004-2007 Mazda3 vehicles because the steering wheel air bag cover may shatter during deployment, projecting plastic fragments into the vehicle.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V495000·2021-07-01

    2021 Chevrolet Silverado 1500 driver air bag may fail to deploy properly

    General Motors is recalling certain 2021 Chevrolet Silverado 1500 vehicles due to a defect in the driver's side frontal air bag module. Missing metal tabs may prevent proper air bag deployment in a crash, increasing the risk of injury.

    Product
    CHEVROLET — CHEVROLET SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V499000·2021-07-01

    Land Rover Recalls 2021 Defender 90 Vehicles for Front Seat Track Defect

    Jaguar Land Rover is recalling 2021 Defender 90 vehicles because a front seat track bracket may deform, preventing the seat from locking and increasing injury risk in a crash.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V497000·2021-07-01

    2021 GMC Canyon Vehicles Recalled for Incorrect Tire Load Capacity Label

    General Motors is recalling 7,199 2021 GMC Canyon vehicles because the tire and loading information placard lists load capacity 51 pounds higher than intended, increasing the risk of vehicle overload and crashes.

    Product
    GMC — GMC CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21759·2021-07-01

    The Best Damn Liquids Liquid Nicotine Recalled for Non-Child-Resistant Packaging

    TBD Liquids is recalling approximately 1,000 units of The Best Damn Liquids branded liquid nicotine because the packaging is not child-resistant as required by law. Liquid nicotine is toxic if swallowed or absorbed through skin or eyes.

    Product
    The Best Damn Liquids branded liquid nicotine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V502000·2021-07-01

    2021 Aprilia Tuono 660 and RS 660 recalled for engine crankshaft defect

    Aprilia is recalling 2021 Tuono 660 and RS 660 motorcycles because the engine crankshaft connecting rod may break due to improper heat-treatment, risking sudden engine stall and crash.

    Product
    APRILIA — APRILIA TUONO 660, RS 660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0688-2021·2021-06-30

    Clio Coconut Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Coconut Less Sugar Yogurt Bars (45g and 50g 10-packs) distributed nationwide due to possible metal fragments in the product.

    Product
    Clio Coconut Less Sugar Yogurt Bars wrapped in a Chocolate Coating 45g x 10 Clio Retail 10-pack and 50g x 10 Clio Retail 10-pack, UPC codes: 854021008237 and 854021008046
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1934-2021·2021-06-30

    Dexcom G6 Sensor 3-Pack Recalled for Temperature-Related Measurement Errors

    Cardinal Health is recalling 2,357 kits of Dexcom G6 Sensor 3-Pack due to temperature exposure during shipping that may cause inaccurate glucose readings. Affected units were distributed in Florida, Georgia, and South Carolina.

    Product
    DEXCOM G6 SENSOR 3 PACK Item Number: 5447552
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1930-2021·2021-06-30

    FREESTYLE LIBRE 14 DAY glucose monitoring system recalled for temperature exposure

    Cardinal Health is recalling 8,959 glucose monitoring kits due to temperature exposure during shipping that may result in inaccurate readings. Affected devices were distributed nationwide.

    Product
    FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084
    Category
    Medical Device
    Distribution
    Distributed nationwide