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.

21576–21600 of 50426

  • HighFDA (Food)·F-0140-2021·2020-12-09

    Minute Maid Strawberry Lemonade Recalled for Metal Fragment

    The Coca-Cola Company is recalling Minute Maid Strawberry Lemonade after a consumer reported a long piece of metal in the product.

    Product
    Minute Maid STRAWBERRY LEMONADE FLAVORED WITH OTHER NATURAL FLAVORS 59 FL OZ (1.8 QT) 1.75 L PRODUCED FOR THE COCA-COLA COMPANY ATLANTA, GA Unit UPC 0 25000 01970 8 Case UPC 000-25000-04812-8
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0528-2021·2020-12-09

    CME America Recalls Neofeed Syringe Pumps Due to Motor Wear and Cracks

    CME America is recalling 4,182 Neofeed syringe pumps because motor wear may cause under-infusion without alarms and cracks may allow cleaning fluids to damage hardware.

    Product
    CME America T-Syringe Pump - Neofeed - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0498-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Infection Risk Mitigation

    Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UCT140P-AL5 - Product Usage: used with other supporting equipment for endoscopic real-time ultrasound imaging and endoscopic surgery within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0532-2021·2020-12-09

    Canon Flat Panel Monitor Recall Due to Cable Breakage Risk

    Canon Medical System is recalling 14 CAS-930A Flat Panel Monitors because the cable may break during procedures, potentially causing delays or vessel damage.

    Product
    CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers: Infinix-8000C and Infinix-8000H - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V761000·2020-12-09

    2021 BMW vehicles recalled for defective 48-Volt battery connections

    BMW is recalling certain 2021 model vehicles due to improper assembly of the 48-Volt battery and starter-generator connection, which can increase electrical resistance and fire risk. Dealers will inspect and replace the connection if necessary.

    Product
    BMW — BMW X5, 530I, X6, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21049·2020-12-09

    GrillBlazer Recalls Propane Torch Guns Due to Fire Hazard

    GrillBlazer is recalling Su-VGun and GrillGun propane torch guns because propane gas can leak, posing a fire hazard. No injuries have been reported.

    Product
    Su-VGun and GrillGun propane torch guns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21045·2020-12-09

    Burley Recalls Dash X FM Child Bicycle Seats Due to Crash Hazard

    Burley is recalling Dash X FM child bicycle seats because the reclining plate can detach, making the seat unstable and causing a crash hazard.

    Product
    Dash® X FM child bicycle seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0530-2021·2020-12-09

    CME America T-Syringe Pump T34 Recalled for Motor Wear and Hardware Cracks

    CME America is recalling 4,182 T-Syringe Pump T34 units because motor wear may cause silent under-infusion and cleaning fluids may crack hardware.

    Product
    CME America T-Syringe Pump - T34 - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20E090000·2020-12-09

    Ford F-250 and F-350 pickup trucks recalled for potential steering lock-up

    Icon Vehicle Dynamics is recalling Ford F-250 and F-350 pickup trucks sold with its centerline stabilizer kit. The foam ring in the shock assembly may block piston ports, causing steering to lock up and increasing crash risk.

    Product
    FORD — FORD F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0504-2021·2020-12-09

    Olympus Ultrasound Endoscope Recall for Infection Risk

    Olympus is recalling ultrasound endoscopes to reduce the risk of patient infections by adding a new inspection step to the cleaning instructions.

    Product
    Olympus Ultrasound Endoscope, Model number: GF-UM160 - Product Usage: used for diagnostic ultrasound imaging or fluid flow analysis of the human body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V757000·2020-12-08

    Grand Design Recalls 2020 Transcend Trailers Due to Gas Leak Risk

    Grand Design is recalling 2020 Transcend recreational trailers because a gas leak at the cook stove joint may increase the risk of fire.

    Product
    GRAND DESIGN — GRAND DESIGN TRANSCEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V756000·2020-12-08

    2019 Mercedes-Benz Sprinter Vehicles Recalled for Inaccurate Operator's Manual

    Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vehicles because the provided operator's manual may contain inaccurate or incomplete safety information.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 4500, SPRINTER 3500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-12082020-01·2020-12-08

    USDA Issues Public Health Alert for Raw Goat Meat Products

    USDA FSIS issued a public health alert for raw goat meat products produced without federal inspection. No confirmed illnesses have been reported.

    Product
    Texas Livestock & Halal Meat Processors — FSIS Issues Public Health Alert for Raw, Fresh Goat Meat Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·20V758000·2020-12-08

    McNeilus Recalls 2020 Bridgemaster V Mixers Due to Missing Axle Information

    McNeilus is recalling 2020 Bridgemaster V Mixer trucks because the required pusher axle operating position is missing from the information plate, increasing crash risk.

    Product
    MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V754000·2020-12-07

    2021 East to West Recreational Trailers: Stowed Grill Fire Hazard

    Forest River is recalling 2021 East to West recreational trailers (approximately 115 units). The grill can be stowed with the propane hose attached and burners on, which can increase fire risk.

    Product
    EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V753000·2020-12-04

    Mercedes-Benz A 220 Recalled for Missing Tire Pressure Labels

    Mercedes-Benz is recalling 2019 A 220 vehicles because missing tire pressure labels may lead to incorrect inflation and increased crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ A 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V752000·2020-12-04

    E-One Recalls Emergency Vehicles Due to Display Lockup Risk

    E-One is recalling specific 2019-2021 emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    E-ONE — E-ONE COMMERCIAL, QUEST II, TYPHOON N, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V751000·2020-12-03

    Land Rover Recalls 2020 Models for Speedometer Display Software Error

    Land Rover is recalling 2020 Discovery Sport and Range Rover Evoque vehicles because a software error may cause the speedometer to randomly switch units, potentially distracting drivers.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE, DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21711·2020-12-03

    Honda Recalls Pioneer 700 and 1000 Vehicles Due to Steering Control Issues

    American Honda is recalling approximately 118,600 Pioneer 700 and 1000 vehicles because the electric power steering system may lose control, posing crash and injury hazards.

    Product
    Honda Pioneer 700 & 1000 Recreational Off-Highway Vehicles (ROVs) with Electric Power Steering (EPS)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0491-2021·2020-12-02

    FDA Recalls Geistlich Bio-Oss Pen Due to Granule Expulsion Risk

    Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen units because granules may be expelled all at once, posing a risk of tissue injury.

    Product
    Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V749000·2020-12-02

    Audi 2021 A6, Q7, RS6, and RS7 Crash Sensor Electrical Defect

    Volkswagen Group of America (Audi) is recalling 2021 Audi A6, Q7, RS6, and RS7 vehicles. An electrical connector can detach from door crash sensors, potentially delaying restraint system activation during side-impact crashes.

    Product
    AUDI — AUDI RS 6 AVANT, RS 7, A6, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0475-2021·2020-12-02

    Conformis Recalls iTotal Hip Replacement System Due to Incorrect Components

    Conformis, Inc. is recalling two iTotal Hip Replacement Systems because incorrect hip components were provided in the kits.

    Product
    iTotal Hip Replacement System, Model number HAA-050-D020-020102 The Conformis Hip System includes standard hip replacement components as well as the following patient specific components: femoral stem and single use instrumentation.
    Category
    Medical Device
    Distribution
    1 state