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.

39976–40000 of 50506

  • HighCPSC·15044·2014-12-09

    Lenovo Recalls Computer Power Cords Due to Fire and Burn Hazards

    Lenovo is recalling LS-15 AC power cords for laptops due to overheating risks that can cause fires and burns. Consumers should stop using the cords and contact Lenovo for a free replacement.

    Product
    AC power cords
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15711·2014-12-09

    Nordstrom Recalls Leith Open Vest Sweaters Due to Burn Hazard

    Nordstrom is recalling Leith brand open vest sweaters because they fail federal flammability standards, posing a burn injury risk. No injuries have been reported.

    Product
    Open Vest Sweaters by Leith
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15043·2014-12-09

    Dream On Me Recalls Play Yards Due to Strangulation Hazard

    Dream On Me is recalling approximately 10,000 Incredible Play Yards because the rails can collapse, posing a strangulation hazard to young children.

    Product
    Dream On Me Play Yards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V782000·2014-12-09

    Starcraft RV Recalls 2015 Launch Ultra Lite Travel Trailers for Tire Label Error

    Starcraft RV is recalling 2015 Launch Ultra Lite travel trailers because tire labels list incorrect pressure information, which could lead to over-inflation and tire blowouts.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH ULTRA LITE, redundant LAUNCH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V780000·2014-12-08

    Kingmor Recalls IC CE School Buses with Cracking Wheelchair Lifts

    Kingmor is recalling 2006-2014 IC CE school buses equipped with certain Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.

    Product
    IC — IC CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V775000·2014-12-05

    Jayco Eagle Fifth Wheel Trailers Recalled for Incorrect Tire Size Labels

    Jayco is recalling 2015 Eagle HT FW 28.5RSTS "PR" trailers because incorrect tire size information on the label could lead to improper tire replacement and increased crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V774000·2014-12-05

    Ford Recalls 2015 Mustangs for Fuel Leak Fire Risk

    Ford is recalling 2015 Mustangs because a fuel pressure sensor may not be seated properly, causing a fuel leak that increases fire risk.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V776000·2014-12-05

    Doubletree RV Recalls 2006-2013 Trailers Due to Door Lock Jamming Risk

    Doubletree RV is recalling 2006-2013 recreational trailers because a defect in the door locks may jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    DOUBLE TREE — DOUBLE TREE MOBILE SUITE, TRADITION, SELECT SUITE, ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15041·2014-12-04

    Salsa Cycles Recalls Bearpaw Bicycle Forks Due to Fall Hazard

    Salsa Cycles is recalling approximately 2,500 Bearpaw bicycle forks because they may bend or break, posing a fall hazard to riders.

    Product
    Salsa Bearpaw Bicycle Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0576-2015·2014-12-03

    Kerry Foods Recalls Meatball Seasoning Due to Salmonella Risk

    Kerry Foods is recalling two meatball seasoning products because they were processed on equipment used for sausage seasoning that tested positive for Salmonella.

    Product
    Kerry 52-0197-02, , Net Wt 39.7 lbs (18.00 Kg), B18516.01.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0474-2015·2014-12-03

    Abbott Recalls ARCHITECT Total T3 Reagent Kits Due to Potential Result Errors

    Abbott Ireland Diagnostics Division is recalling 7,415 ARCHITECT Total T3 Reagent Kits because 17% of specific lots may produce patient results higher than expected.

    Product
    ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated microparticles in MES buffer with sheep IgG stabilizers. Minimum Concentration: 0.08% solids. Preservative: ProClin 300. - 1 or 4 Bottle(s) (5.9 mL/26.3 mL) T3…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0565-2015·2014-12-03

    Los Chileros Blue Corn Waffle Mix Recalled for Undeclared Wheat

    Los Chileros De Nuevo Mexico is recalling Blue Corn Waffle & Pancake Mix and six other products due to undeclared wheat.

    Product
    Los Chileros de nuevo mexico gourmet southwestern cuisine Blue Corn Waffle & Pancake Mix, Net Wt. 16 oz (453.6 grams), Los Chileros de Nuevo Mexico, PO Box 6215, Santa Fe, NM 87502
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0440-2015·2014-12-03

    Intuitive Surgical Recalls 8mm Cardiac Probe Grasper Due to Reprocessing Deviations

    Intuitive Surgical is recalling 509 units of 8mm Cardiac Probe Graspers because deviations in reprocessing steps can cause surface degradation and accelerated mechanical wear.

    Product
    8MM, CARDIAC PROBE GRASPER; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0569-2015·2014-12-03

    Los Chileros Recalls Multiple Southwestern Food Products for Undeclared Wheat

    Los Chileros De Nuevo Mexico is recalling seven food products, including Carne Adovada and Sopaipilla Mix, due to undeclared wheat.

    Product
    Los Chileros de nuevo mexico gourmet southwestern cuisine Carne Adovada with Sopaipilla Mix, 13 oz.., Los Chileros de Nuevo Mexico, PO Box 6215, Santa Fe, NM 87502
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0468-2015·2014-12-03

    Summit J700 X-Ray Tube Stand Recalled for Insufficient Welds

    Summit Industries is recalling 32 J700 Floor Mounted Tube Stands because insufficient welds may cause breakage, leading to equipment damage or injury.

    Product
    The J700 Floor Mounted Tube Stand (FMTS) is intended to support and position the diagnostic x-ray tube housing assembly for a medical radiographic procedure. The product consists of a vertical column (with counterbalanced vertical carriage, counterweight and pulley system)…
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-0428-2015·2014-12-03

    Intuitive Surgical Recalls 8mm Large Needle Driver Instruments

    Intuitive Surgical is recalling 509 8mm Large Needle Driver instruments due to potential surface degradation and accelerated mechanical wear caused by reprocessing deviations.

    Product
    8MM,LARGE NEEDLE DRIVER; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0427-2015·2014-12-03

    Intuitive Surgical Recalls 8mm Potts Scissors Due to Reprocessing Deviations

    Intuitive Surgical is recalling 509 8mm Potts Scissors because deviations in reprocessing steps can cause surface degradation and accelerated mechanical wear.

    Product
    8MM,POTTS SCISSORS; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0447-2015·2014-12-03

    Intuitive Surgical Recalls 8mm Curved Bipolar Dissectors Due to Reprocessing Deviations

    Intuitive Surgical is recalling 509 units of 8mm Curved Bipolar Dissectors because deviations in reprocessing steps can cause surface degradation and mechanical wear.

    Product
    8MM, CURVED BIPOLAR DISSECTOR; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0429-2015·2014-12-03

    Intuitive Surgical Recalls 8mm Black Diamond Micro Forceps Due to Reprocessing Deviations

    Intuitive Surgical is recalling 509 units of 8mm Black Diamond Micro Forceps because deviations in reprocessing steps can cause surface degradation and accelerated mechanical wear.

    Product
    8MM,BLACK DIAMOND MICRO FORCEPS; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0485-2015·2014-12-03

    Respironics Esprit V1000 Ventilator Recall for Power Supply Defect

    Respironics is recalling Esprit V1000 and V200 Conversion Ventilators because incorrect screw installation may cause a short circuit, preventing the switch to battery power during AC outages.

    Product
    Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V1000 and Esprit/V200 Conversion Ventilators are microprocessor-controlled, electrically powered mechanical ventilators. Intended for use by medical personnel to provide continuous or intermittent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0570-2015·2014-12-03

    Los Chileros Recalls Multiple Foods for Undeclared Wheat Allergen

    Los Chileros De Nuevo Mexico is recalling seven food products, including soups and mixes, due to undeclared wheat.

    Product
    Los Chileros de nuevo mexico gourmet southwestern cuisine Cream of Green Chile Chicken Soup, 5.92 oz.., Los Chileros de Nuevo Mexico, PO Box 6215, Santa Fe, NM 87502
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0471-2015·2014-12-03

    Toshiba Cardiac Function Analysis Software Recalled for Incorrect Results

    Toshiba American Medical Systems is recalling one unit of cardiac function analysis software in the US because it may display incorrect analysis results.

    Product
    Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A The software is applicable to the following CT systems: Aquilion ONE TSX-301C X-ray CT system with a 320-row 0.5 mm detector is provided with a 7.5-MHU large-capacity X-ray tube unit, and permits…
    Category
    Medical Device
    Distribution
    Distributed nationwide