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.

28051–28075 of 32242

  • SevereNHTSA·13V291000·2013-07-02

    Chrysler Recalls 2013 Minivans Due to Air Bag Software Defect

    Chrysler is recalling 2013 Town & Country and Dodge Grand Caravan minivans because incorrect software in the occupant restraint control module may affect air bag deployment.

    Product
    DODGE — DODGE, CHRYSLER GRAND CARAVAN, TOWN AND COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V282000·2013-07-02

    Chrysler Recalls 2011-2013 Vehicles for Active Head Restraint Defect

    Chrysler is recalling specific 2011-2013 models because electrical issues may prevent active head restraints from deploying in rear-end collisions, increasing injury risk.

    Product
    DODGE — DODGE, JEEP, CHRYSLER AVENGER, LIBERTY, 200, SEBRING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V284000·2013-07-01

    Monaco RV Recalls 2,250 Vehicles Due to Water Tank Mounting Failure

    Monaco RV is recalling 2,250 recreational vehicles because the water tank mounting system may fail, causing the tank to separate and become a road hazard.

    Product
    R-VISION — R-VISION, MCKENZIE, HOLIDAY RAMBLER TRAIL SPORT, ONYX, RAINIER ASCENT, ALUMA-LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V276000·2013-06-28

    Altec Lift-All LSS Aerial Devices Recalled for Turntable Cracks

    Altec is recalling 2008-2009 Lift-All LSS aerial devices because cracks in the turntable may cause failure, increasing the risk of personal injury.

    Product
    ALTEC LLC — ALTEC LLC LIFT-ALL LSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V271000·2013-06-27

    GM Recalls 2012 Chevrolet Volt for Brake Pressure Valve Defect

    General Motors is recalling specific 2012 Chevrolet Volt vehicles because a brake pressure modulator valve issue may cause front brakes to lock up during safety system events.

    Product
    CHEVROLET — CHEVROLET VOLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V281000·2013-06-27

    La Boit Recalls 2013 Mobile Services Vehicles Due to Awning Motor Defect

    La Boit is recalling 2013 Mobile Services vehicles because power awning motor screws may shear, causing the awning to unfurl unexpectedly and increasing crash risk.

    Product
    LA BOIT — LA BOIT MOBILE SERVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V274000·2013-06-27

    Amerivan Toyota Sienna Vans Recalled for Fuel Filler Neck Contact

    Eldorado National is recalling 2011-2013 Amerivan Toyota Sienna vans because the fuel filler neck may contact the shock absorber, risking a fire.

    Product
    AMERIVAN — AMERIVAN TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1558-2013·2013-06-26

    Verathon Recalls GlideScope Reusable Laryngoscope Blades Due to Breakage Risk

    Verathon is recalling GlideScope reusable laryngoscope blades because the tips may break prematurely without visible signs, posing a risk to patients during intubation.

    Product
    GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The GlideScope Video Laryngoscopes are intended for use by qualified medical professionals to obtain a clear, unobstructed view of the vocal cords for medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-609-2013·2013-06-26

    Pharmacia Recalls Cleocin Phosphate Vials Due to Glass Delamination

    Pharmacia & Upjohn LLC is recalling specific lots of Cleocin Phosphate injection vials due to the presence of very small reflective flakes consistent with glass delamination.

    Product
    CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V268000·2013-06-26

    Volvo Trucks Recall 2007-2014 Models Due to Clutch Disengagement Defect

    Volvo is recalling 23,056 heavy-duty trucks from 2007-2014 because a missing redundant switch may prevent the clutch from disengaging, increasing stopping distance.

    Product
    VOLVO — VOLVO VNL, VNM, VT, VAH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1533-2013·2013-06-26

    Lightlife Veggie Burgers Recalled for Undeclared Milk Allergen

    Conagra is recalling Lightlife Farmer's Market Veggie Burgers because packaging may contain milk-containing products, and the milk allergen is not declared on the label.

    Product
    Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed By: Lightlife Foods, Turners Falls, MA. Case UPC Code: 20043454805252
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Drugs)·D-606-2013·2013-06-26

    Teva Recalls Actiq Fentanyl Lozenges Due to Dissolution Failure

    Teva Pharmaceuticals is recalling 316 cartons of Actiq 200 mcg fentanyl lozenges because they failed dissolution specifications during stability testing.

    Product
    Actiq (oral transmucosal fentanyl citrate) 200 mcg, lozenge on a stick, a)Single Blister (NDC 63459-502-01), b) 30 count carton (NDC 63459-502-30), Rx only, Manufactured by: Cephalon, Inc., Salt Lake City, UT 84116
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-605-2013·2013-06-26

    Sagent Recalls Vecuronium Bromide Injection Due to Manufacturing Deviations

    Sagent Pharmaceuticals is recalling Vecuronium Bromide for Injection because it was not manufactured under current good manufacturing practices, resulting in failed impurity specifications.

    Product
    VECURONIUM Bromide for Injection, 10 mg* per vial, *1 mg per mL when reconstituted to 10 mL, for IV single use only, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195 (USA); Mfd. by MN Pharmaceuticals; Made in Turkey, NDC 25021-657-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1537-2013·2013-06-26

    Respironics V60 Ventilator Recalled for Power Management Board Software Issue

    Respironics is recalling V60 ventilators due to a software issue on the Power Management Board Assembly that could cause loss of ventilator support without an audible alarm.

    Product
    Respironics V60 Ventilator, Model #V60 Respironics Material P/N (Philips 12 Digit P/N): 85008 (85008) 1053613 (989805628251) 1053614 (989805612101) 1053615 (989805613391) 1053616 (989805613661) 1053617 (989805611761) 1053618 (n/a) R1053618 (n/a) 1076709 (n/a)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1548-2013·2013-06-26

    Biomet Recalls Superior Approach Resection Guide Assembly Due to Slot Offset

    Biomet is recalling 17 units of the Superior Approach Resection Guide Assembly because a manufacturing defect may prevent the guide from securing properly to bone during surgery.

    Product
    Superior Approach Resection Guide Assembly. Indicated for primary, fracture, or revision total shoulder replacement for the relief of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1544-2013·2013-06-26

    Julian's Recipe Pretzel Baguette Recalled for Undeclared Soy Flour

    Julian's Recipe is recalling specific lots of European Style Pretzel Baguettes due to an undeclared soy flour ingredient caused by a repacking error.

    Product
    ALL NATURAL Julian's RECIPE European Style Pretzel Baguette, BUTTER & SEA SALT, NET WT 11.3 OZ (320 g), UPC 8 55971 00226 9, 2 BAGUETTES, KEEP FROZEN -- Product of Germany. Manufactured for Distribution by Julian's Recipe, LLC PO Box 323, Montgomery, NY 12549. --- The product…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-608-2013·2013-06-26

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Sterility Concerns

    Hospira is recalling 676,872 containers of 0.9% Sodium Chloride Injection due to a potential leak at the administrative port that compromises sterility.

    Product
    0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·13225·2013-06-25

    Bel Air Lighting Recalls Chandeliers Due to Falling Hazard

    Bel Air Lighting is recalling about 20,500 nine-light chandeliers because the mounting loop can break, causing the fixture to fall and pose an impact injury hazard.

    Product
    Portfolio and Transglobe nine-light chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V260000·2013-06-24

    Honda Recalls 2007-2008 Fit Vehicles for Power Window Fire Risk

    Honda is re-recalling 2007-2008 Fit vehicles because water intrusion can damage the power window switch, potentially causing overheating, smoke, and fire.

    Product
    HONDA — HONDA FIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V253000·2013-06-21

    Elkhart Coach Shuttle Bus Recall for Wheelchair Lift Fire Risk

    Elkhart Coach is recalling 2006-2012 shuttle buses because a wheelchair lift cable may cause a short circuit and fire.

    Product
    ELKHART COACH — ELKHART COACH SHUTTLE BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V258000·2013-06-21

    Vermeer Recalls 2012-2013 R9X12T Trailers Due to Air Brake Defect

    Vermeer is recalling 2012-2013 R9X12T trailers because an incorrectly installed air-brake booster valve may increase stopping distances, raising the risk of a crash.

    Product
    VERMEER — VERMEER R9X12T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V261000·2013-06-21

    Mobility Works Recalls Ford E-Series Vans with Wheelchair Lift Fire Risk

    Mobility Works is recalling 2006-2012 Ford E-150, E-250, and E-350 vans equipped with specific wheelchair lifts due to a potential fire hazard from cable contact.

    Product
    FORD — FORD E-350, E-250, E-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E035000·2013-06-21

    Sutrak HVAC Systems Recalled for Potential Fire Risk in DART Buses

    Sutrak USA is recalling HVAC systems used in DART 39000 buses because a fuse holder defect may allow voltage spikes that damage electrical components and cause a fire.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide