The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

19976–20000 of 32117

  • SevereNHTSA·16V479000·2016-06-28

    Ford Recalls 2015-2016 Focus Electric Vehicles for Transmission Defect

    Ford is recalling 865 model year 2015-2016 Focus Electric vehicles because the transmission's differential pinion gear shaft may overheat and fracture, potentially causing a loss of motive power and park function.

    Product
    FORD — FORD FOCUS ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V474000·2016-06-28

    Cheetah Chassis Recalls Trailers Due to Spring Brake Valve Defect

    Cheetah Chassis is recalling specific 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    CHEETAH — CHEETAH FLATBED TRAILER, EXTENDABLE CHASSIS, BRIDGEMASTER CHASSIS, CURTAINSIDE FLATBED
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V472000·2016-06-28

    Forest River Charleston Motorhomes Recalled for Throttle Sensor Defect

    Forest River is recalling 2014-2016 Charleston motorhomes because a throttle sensor defect may prevent the engine brake from activating, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHARLESTON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V468000·2016-06-27

    Thor Motor Coach Recalls Motorhomes Due to Front Sway Bar Defect

    Thor Motor Coach is recalling 2016-2017 Venetian, Tuscany, and Palazzo motorhomes because front sway bar brackets may not fit properly, risking detachment and crashes.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR VENETIAN, TUSCANY, PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V467000·2016-06-27

    Volvo Recalls 2013 VNM and VNL Trucks for Front Axle Defect

    Volvo is recalling 129 model year 2013 VNM and VNL trucks because certain front steer axles may fracture, increasing the risk of a crash.

    Product
    VOLVO — VOLVO VNM, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V470000·2016-06-27

    John Evans Recalls 2016 Cheetah Flatbeds Due to Brake Drag Risk

    John Evans is recalling 2016 Cheetah tandem flatbed trailers because a defective brake actuator may cause brake drag, potentially leading to a wheel end fire.

    Product
    JOHN EVANS — JOHN EVANS CHEETAH TANDEM FLATBED
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V486000·2016-06-27

    Vermeer Recalls Trailers Due to Spring Brake Valve Defect

    Vermeer is recalling specific 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    VERMEER — VERMEER HG4000, DT6, WC2500XL, TG5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·053-2016·2016-06-26

    Ghiringhelli Recalls Chicken Caesar Salad Due to Undeclared Allergens

    Ghiringhelli Specialty Foods is recalling approximately 2,444 pounds of Trader Giotto's Chicken Caesar Salad because the products contain undeclared soy, wheat, and fish, and are missing a shellfish warning.

    Product
    Ghiringhelli Brothers — Ghiringhelli Specialty Foods, Inc. Recalls Poultry Products Due To Mislabeling and Undeclared Allergens
    Category
    Food
    Distribution
    10 states
  • SevereUSDA FSIS·052-2016 EXP·2016-06-25

    U.S. Cado Holdings Recalls Imported Swai Fillets for Import Violations

    U.S. Cado Holdings is recalling approximately 27,995 pounds of imported frozen Swai fillets that entered U.S. commerce without meeting federal residue testing requirements.

    Product
    U.S. Cado Holdings, Inc. Recalls Imported Siluriformes Fish Products Distributed Without Meeting FSIS Requirements
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·16V461000·2016-06-24

    Chrysler Recalls 2015-2016 Vehicles for Transmission Pump Defect

    Chrysler is recalling specific 2015-2016 Town & Country, Grand Caravan, Journey, and ProMaster vehicles because a transmission pump may seize, causing loss of motive power and increasing crash risk.

    Product
    DODGE — DODGE, RAM, CHRYSLER GRAND CARAVAN, PROMASTER, JOURNEY, TOWN AND COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V458000·2016-06-23

    Mitsubishi Recalls Vehicles for Front Control Arm Corrosion Risk

    Mitsubishi is recalling specific Lancer and Outlander models because front cross members may corrode, causing control arms to detach and increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, LANCER WAGON, LANCER EVOLUTION, LANCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1888-2016·2016-06-22

    CareFusion Recalls AVEA Ventilators Due to Fuse Defect

    CareFusion is recalling AVEA Comprehensive ventilators because an incorrect fuse may fail, causing loss of power to the user interface module.

    Product
    AVEA Comprehensive ventilator, 17310-xx (xx = 0 - 14) A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V457000·2016-06-22

    Forest River Recalls 2013-2016 XLR Toyhaulers for Axle Bolt Defect

    Forest River is recalling 2013-2016 XLR toyhaulers because improperly seated axle bolts may allow the axle to shift, increasing the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1894-2016·2016-06-22

    CareFusion Recalls AVEA Ventilators Due to Fuse Defect

    CareFusion is recalling AVEA Ventilators because a defective fuse on the TCA Board may fail, causing loss of power to the User Interface Module.

    Product
    TCA Board, 16542A A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1899-2016·2016-06-22

    CareFusion Recalls AVEA Ventilator Upgrade Kits Due to Fuse Defect

    CareFusion is recalling AVEA GDE upgrade kits because an incorrect fuse may fail, causing loss of power to the ventilator's user interface.

    Product
    AVEA GDE upgrade kit, 12284-PMN A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1037-2016·2016-06-22

    Fresenius Kabi Recalls Sensorcaine Due to Glass Particulate Matter

    Fresenius Kabi is recalling specific lots of Sensorcaine injection because glass particulate matter was found in the sterile product.

    Product
    SENSORCAINE — SENSORCAINE (BUPIVACAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1889-2016·2016-06-22

    CareFusion Recalls AVEA Standard Ventilators Due to Fuse Defect

    CareFusion is recalling AVEA Standard ventilators because an incorrect fuse may fail, causing a loss of power to the user interface module.

    Product
    AVEA Standard ventilator, 17311-xx (xx = 0 - 14) A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1898-2016·2016-06-22

    CareFusion Recalls AVEA Ventilator Upgrade Kits Due to Fuse Defect

    CareFusion is recalling AVEA Ventilator upgrade kits because an incorrect fuse may fail, causing loss of power to the User Interface Module.

    Product
    AVEA GDE/UIM upgrade kit, 12283-PMN A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1897-2016·2016-06-22

    CareFusion Recalls AVEA Ventilators Due to Fuse Failure Risk

    CareFusion is recalling 922 AVEA Ventilators worldwide because an incorrect fuse may fail, causing loss of power to the user interface module.

    Product
    Gas Delivery Engine (GDE)-refurbished, R16650A A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V456000·2016-06-22

    Mack Recalls 2013 Pinnacle Trucks Due to Front Axle Fracture Risk

    Mack Trucks is recalling 2013 Pinnacle (CXU) trucks because improperly heat-treated front axles may fracture, increasing the risk of a crash.

    Product
    MACK — MACK PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1978-2016·2016-06-22

    Navilyst Recalls Xcela Hybrid PICC Catheters Due to Hemolysis Risk

    Navilyst Medical is recalling specific Xcela Hybrid PICC catheters manufactured before July 15, 2014, because they lack a specification change that reduces hemolysis during blood sampling.

    Product
    Xcela Hybrid PICC with PASV Valve Technology, IR-145 Kit, 6F-55cm, UPN H965952430 & H965952470, Rx ONLY The Xcela PICC with PASV, Xcela Hybrid PICC with PASV, BioFlo PICC with PASV and BioFlo Hybrid PICC with PASV are indicated for short or long-term peripheral access to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1890-2016·2016-06-22

    CareFusion Recalls AVEA Standard Ventilators Due to Fuse Defect

    CareFusion is recalling AVEA Standard ventilators because an incorrect fuse may fail, causing loss of power to the user interface module.

    Product
    AVEA Standard with Compressor ventilator, 17312-xx (xx = 0 - 14) A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas.
    Category
    Medical Device
    Distribution
    Distributed nationwide