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.

31926–31950 of 50502

  • HighNHTSA·17V416000·2017-06-29

    Toyota Recalls 2016 Tundra Vehicles Due to Passenger Knee Air Bag Bolt Issue

    Toyota is recalling 2016 Tundra vehicles because incorrect bolts were used to attach the passenger knee air bag module, which may loosen over time and affect air bag performance during a crash.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2602-2017·2017-06-28

    Medtronic Recalls MiniMed 620G Insulin Pumps Due to Keypad Malfunction

    Medtronic is recalling 6,573 MiniMed 620G insulin infusion pumps because the keypad may become unresponsive and the pump may become temporarily stuck.

    Product
    MiniMed 620G Insulin Infusion Pump, Catalog No. MMT-1510, MMT-1710, MMT-1550, MMT-1750.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2386-2017·2017-06-28

    Publix Deli Artichoke and Spinach Dip Recalled for Glass Fragments

    Publix Super Markets is recalling 16-ounce Artichoke & Spinach dip due to potential glass fragments. The product was distributed to six southeastern states.

    Product
    Publix Deli, Artichoke & Spinach dip, 16 oz., plastic clamshell, Manufactured and distributed by Publix Super Markets, Lakeland, FL.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-2390-2017·2017-06-28

    Southern Grove Cashew Halves Recalled for Glass Fragment Risk

    Star Snacks Co. is recalling Southern Grove Cashew Halves & Pieces with Sea Salt because a consumer found a glass fragment in the product.

    Product
    Southern Grove Cashew Halves & Pieces with Sea Salt, Net Weight 8.0 oz. (227 grams)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2605-2017·2017-06-28

    Medtronic Recalls MiniMed 670G Insulin Pumps Due to Keypad Issues

    Medtronic is recalling 117,239 MiniMed 670G insulin pumps because the keypad may become unresponsive and the pump may become temporarily stuck.

    Product
    MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2375-2017·2017-06-28

    Meijer Honey Vanilla Bourbon Pecans Recalled for Mislabeling

    Meijer is recalling Honey Vanilla Bourbon Pecans because the label incorrectly lists cream, milk, and eggs, while omitting other ingredients.

    Product
    Meijer Honey Vanilla Bourbon Pecans, 8.5 oz., 6/case, packed in a stand-up pouch.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2619-2017·2017-06-28

    DePuy Mitek LATARJET Extraction Driver Recalled for Breakage Risk

    DePuy Mitek is recalling 115 units of the LATARJET EXPERIENCE Extraction Driver because the tip may break during surgery when used at an angle.

    Product
    DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2621-2017·2017-06-28

    Omega Medical Imaging Recalls Elevating Monitor Suspension Pillars

    Omega Medical Imaging is recalling 6 units of 2 over 2 Elevating Monitor Suspension pillars because the column may drop and fail to rise.

    Product
    Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that elevates monitor for healthcare professionals.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-2377-2017·2017-06-28

    Hail Merry Meyer Lemon Mini Tarts Recalled for Undeclared Cashews

    Hail Merry LLC is recalling Meyer Lemon Miracle Mini Tarts due to undeclared cashews. Consumers should check for specific lot codes.

    Product
    Hail Merry Meyer Lemon Miracle Mini Tarts, 6 tartlets per tray packaged in clear plastic molded trays.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2603-2017·2017-06-28

    Medtronic Recalls MiniMed 630G Insulin Pumps Due to Keypad Malfunction

    Medtronic is recalling 65,959 MiniMed 630G insulin pumps because the device may become temporarily stuck and the keypad may become unresponsive.

    Product
    MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2618-2017·2017-06-28

    DePuy Mitek Top Hat Tap Screw Driver Tip Recall

    DePuy Mitek is recalling 153 units of the LATARJET EXPERIENCE Top Hat Tap because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2604-2017·2017-06-28

    Medtronic Recalls MiniMed 640G Insulin Pumps Due to Keypad Malfunction

    Medtronic is recalling 117,239 MiniMed 640G insulin pumps because the keypad may become unresponsive, potentially preventing users from adjusting insulin delivery.

    Product
    MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·17V409000·2017-06-28

    KME Predator Tanker Recalled for Fuel Pump Drive Gear Slip

    Kovatch Mobile Equipment is recalling one 2017 KME Predator Tanker truck because a fuel pump drive gear may slip, causing an engine stall that increases crash risk.

    Product
    KME — KME PREDATOR TANKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2592-2017·2017-06-28

    Ion Beam Applications Recalls Proteus 235 Medical Devices

    Ion Beam Applications S.A. is recalling 18 Proteus 235 systems due to potential dark current issues in Pencil Beam Scanning mode.

    Product
    Proteus 235
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-2374-2017·2017-06-28

    Joray Fruit Punch Fruit Rolls Recalled for Undeclared Wheat

    Joseph Shalhoub & Son, Inc. is recalling Joray Fruit Punch fruit rolls because they contain undeclared wheat. The product was distributed in New York and Florida.

    Product
    joray fruit roll  FRUIT PUNCH flavor NET WT 1 OZ. (28g). UPC# 0 51063 50009 9.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2615-2017·2017-06-28

    DePuy Mitek LATARJET Combo Screw Driver Recalled for Breakage Risk

    DePuy Mitek is recalling 173 LATARJET Combo Screw Drivers because the tip may break during surgery when used at an angle.

    Product
    DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighNHTSA·17V407000·2017-06-28

    Lance Recalls 2018 Travel Trailers with Defective Utility Receivers

    Lance is recalling 2018 Travel Trailers with optional utility receivers that have insufficient welds, which may cause attached items to contact the road.

    Product
    LANCE — LANCE TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V405000·2017-06-27

    Triple E RV Recalls 2017 Wonder Motorhomes Due to Fire Risk

    Triple E RV is recalling 35 units of the 2017 Wonder motorhome because the water heater door can block the furnace, increasing fire risk.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V404000·2017-06-27

    GM Recalls 2016-2017 Buick Envision for Head Restraint Defect

    General Motors is recalling 2016-2017 Buick Envision vehicles because incorrectly installed tablet holders may prevent head restraints from fully engaging, increasing injury risk in a crash.

    Product
    BUICK — BUICK ENVISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V400000·2017-06-26

    Audi Recalls 2016-2017 Q3 Models Due to Brake Light Software Defect

    Volkswagen Group of America is recalling 2016-2017 Audi Q3 vehicles because brake lights may not activate during emergency braking if the parking brake is engaged.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V393000·2017-06-22

    Mazda Recalls 2014-2016 Mazda3 and Mazda6 for Parking Brake Defect

    Mazda is recalling 2014-2016 Mazda3 and Mazda6 vehicles because water may cause the parking brake actuator shaft to corrode and bind, potentially preventing the brake from engaging or disengaging fully.

    Product
    MAZDA — MAZDA MAZDA6, MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V394000·2017-06-22

    Jaguar Recalls 2010-2011 XJ Vehicles for Air Bag Software Defect

    Jaguar is recalling 2010-2011 XJ vehicles because a software update failure may leave air bag calibration incorrect, increasing injury risk in a crash.

    Product
    JAGUAR — JAGUAR XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide