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.

13451–13475 of 29188

  • SevereNHTSA·18V759000·2018-10-29

    2018 Jeep Grand Cherokee SRT and Trackhawk Floor Mat Recall

    Chrysler is recalling 2018 Jeep Grand Cherokee SRT and Trackhawk vehicles because the driver's floor mat may prevent the accelerator pedal from returning to idle, increasing crash risk.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·106-2018·2018-10-27

    Red Square Foods Recalls Frozen Meat and Poultry Products for Undeclared Allergens

    Red Square Foods is recalling frozen meat and poultry ravioli and blintzes because they contain undeclared eggs, milk, and wheat.

    Product
    Red Square Foods, Inc., Recalls Frozen Not-Ready-To-Eat Meat and Poultry Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·18V757000·2018-10-26

    Altec Recalls 2018 Digger Derricks and Aerial Devices for Fastener Failure

    Altec is recalling 2018 Digger Derricks and Aerial Devices because high-strength fasteners may fail, causing the pedestal to separate from the turn table and increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V755000·2018-10-25

    BMW Recalls Diesel Vehicles Due to EGR Cooler Leak Fire Risk

    BMW is recalling specific 2013-2018 diesel models because a leaking EGR cooler can cause the intake manifold to melt, increasing the risk of a fire.

    Product
    BMW — BMW 328D, X5, 535D, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V754000·2018-10-25

    Kia Recalls 2018 Stinger Vehicles Due to Wiring Fire Risk

    Kia is recalling 2018 Stinger vehicles because a front wiring harness may be damaged by a burr, increasing the risk of a fire.

    Product
    KIA — KIA STINGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19015·2018-10-25

    Haier Top-Mount Refrigerators Recalled Due to Fire Hazard

    Haier America is recalling about 137,000 top-mount refrigerators because an electrical component can short circuit, posing a fire hazard.

    Product
    Haier Top-Mount Refrigerators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0071-2019·2018-10-24

    CeraVe Healing Lip Balm Recalled for Staphylococcus Aureus Contamination

    Product Quest Manufacturing LLC is recalling CeraVe Healing Lip Balm/SPF 30 due to failed microbiological testing for Staphylococcus aureus.

    Product
    CeraVe Healing Lip Balm/SPF 30 (avobenzone 3%, dimethicone 1%, homosalate 10%, octisalate 5%, octocrylene 10%, Net Wt. 0.15 oz. (4.25 g) stick, CeraVe LLC., New York, NY 10001, UPC 3 01872 49201 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0039-2019·2018-10-24

    Harmon Face Values Saline Nasal Gel Recalled for Quality Deviations

    Product Quest Manufacturing LLC is recalling Harmon Face Values Saline Nasal Gel with Soothing Aloe due to manufacturing deviations that could impact product quality.

    Product
    Harmon Face Values, Saline Nasal Gel with Soothing Aloe, 0.5 oz. (14.1 g) tube, Distributed by: Harmon Stores, Inc., Union, NJ 07083 USA, UPC 7 27510 00474 7 .
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0027-2019·2018-10-24

    Dermatone Sunscreen Stick Recalled for Staphylococcus Aureus Contamination

    Product Quest Manufacturing LLC is recalling Dermatone No-Touch Sunscreen Sticks because samples tested positive for Staphylococcus aureus.

    Product
    DERMATONE (titanium oxide 6% and zinc oxide 4.7%) No-Touch Sunscreen Stick, SPF 50, Net Wt. 0.49 oz. (13.9g) stick, Distributed by: Beaumont Products, Inc. Kennesaw, GA 30144, UPC 0 20908 05100 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0103-2019·2018-10-24

    Thoratec CentriMag Motor Recall Due to Electrical Cable Failure

    Thoratec is recalling CentriMag Motors because a wire break or short circuit in the cable can cause the motor to stop.

    Product
    Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood Pumping System.
    Category
    Medical Device
    Distribution
    43 states
  • SevereFDA (Drugs)·D-0062-2019·2018-10-24

    Product Quest Recalls Well at Walgreens Sinus Relief Mist for Quality Issues

    Product Quest Manufacturing LLC is recalling Well at Walgreens ULTRA FINE Sinus Relief Mist due to manufacturing deviations that could impact product quality.

    Product
    Well at Walgreens, ULTRA FINE Sinus Relief Mist (Oxymetazoline HCl 0.05%) bottle, Sinus Reliever, Nasal Decongestant, 12 Hour Pump Mist, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7000-01, UPC 3 11917 18535 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0066-2019·2018-10-24

    Freeze It Spray Recalled for High Camphor Levels

    Product Quest Manufacturing LLC is recalling Freeze It spray cans due to high out-of-specification camphor levels.

    Product
    FREEZE IT (camphor 0.2% and menthol 3.5%) spray, 118.29 mL (4 fl. oz.) can, Distributed by: Expedite Products, Inc., Tampa, FL 33619 USA, UPC 8 56569 00203 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0063-2019·2018-10-24

    Walgreens Anefrin Nasal Spray Recalled for Manufacturing Quality Issues

    Product Quest Manufacturing LLC is recalling 355,056 bottles of Walgreens Anefrin Nasal Spray due to manufacturing conditions that could impact product quality.

    Product
    Walgreens, NO DRIP, Anefrin Nasal Spray (Oxymetazoline HCl 0.05%), Nasal Decongestant, Original, 12 Hour, Maximum Strength, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015,NDC 0363-7005-01, UPC 3 11917 18537 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0181-2019·2018-10-24

    OriGen Biomedical Recalls Reinforced Dual Lumen Cannulas Due to Deficiencies

    OriGen Biomedical is recalling 435 Reinforced Dual Lumen Cannulas because they may lack barium sulfate and have tips shorter than labeled.

    Product
    Reinforced Dual Lumen Cannula, 19Fr., REF: VV19F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0178-2019·2018-10-24

    Siemens Biograph mCT PET/CT Scanners Recalled for Plug Overheating Risk

    Siemens Medical Solutions is recalling 890 Biograph mCT PET/CT scanners because plug terminals may become loose and overheat.

    Product
    Biograph mCT: a) S(64)-3R, Material Number 10248669 b) S (20) -3R, Material Number 10507786 c) Flow 20-4R, Material Number 10528958 d) m Flow 64-4R, Material Number 10529161 e) mCT S(40)-4R, Material Number 10248671 f) mCT S(64)-4R, Material Number 0248672 g) mCT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0072-2019·2018-10-24

    Mushatt's No. 9 PsoriWash Medicated Wash Recalled for Microbial Contamination

    Product Quest Manufacturing LLC is recalling Mushatt's No. 9 PsoriWash Medicated Wash due to microbial contamination and low salicylic acid levels.

    Product
    Mushatt's No. 9, PsoriWash Medicated Wash, Salicylic Acid 1.8%, 8 oz. (226 g) tube, Distributed by Mushatts, LLC, P.O. Box 372476, Satellite Beach, FL 32937, UPC 8 58245 00203 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0029-2019·2018-10-24

    Product Quest Recalls CareOne Saline Nasal Gel Due to Quality Concerns

    Product Quest Manufacturing LLC is recalling CareOne Saline Nasal Gel With Soothing Aloe because it was manufactured under conditions that could impact product quality.

    Product
    CareOne, Saline Nasal Gel With Soothing Aloe, Net Wt. 0.5 OZ (14.1 g) tube, Distributed by Foodhold U.S.A., LLC., Landover, MD 20785, 1-877-846-9949, UPC 3 41520 00175 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0050-2019·2018-10-24

    Sweet Me Creamery Brookie Dough Ice Cream Recalled for Undeclared Peanuts

    Kemps, LLC is recalling Sweet Me Creamery Brookie Dough ice cream because it may contain undeclared peanuts. The product was distributed in Illinois, Minnesota, North Dakota, and Wisconsin.

    Product
    Sweet Me Creamery Brookie Dough ice cream, packaged in following configuration: 1 Pint (473 ML), UPC: 41483-04219 or 4-Pack of 1 Pint (473 ML) containers Net Half Gallon (1.89L), UPC 41483-04241. Vanilla ice cream swirled with sea salt fudge and pieces of cookie dough and…
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·18V750000·2018-10-23

    Proterra Recalls 2016-2017 Catalyst Buses Due to Brake Caliper Defect

    Proterra is recalling 2016-2017 Catalyst transit buses because a defect in the brake calipers may cause the guide pin support bolt to break, potentially leading to loss of braking ability or tire pressure.

    Product
    PROTERRA — PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V748000·2018-10-22

    E-One Recalls 2016-2018 Typhoon and Cyclone II Aerial Devices

    E-One is recalling 2016-2018 Typhoon and Cyclone II aerial devices because a torque rod tower may crack, potentially affecting vehicle handling and increasing crash risk.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V747000·2018-10-22

    E-One Recalls 2012-2015 Emergency Vehicles Due to Fire Risk

    E-One is recalling 2012-2015 Typhoon, Cyclone II, and Cyclone III emergency vehicles because a melting relay in the HVAC system can increase the risk of a fire.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON, CYCLONE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V735000·2018-10-22

    Ford Recalls 2012-2018 Focus Models Due to Fuel System Defect

    Ford is recalling 2012-2018 Focus vehicles with 2.0L engines because a malfunctioning valve may cause the engine to stall while driving, increasing crash risk.

    Product
    FORD — FORD FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide