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.

13251–13275 of 29186

  • SevereFDA (Food)·F-0611-2019·2018-11-21

    Ukrop's Ham on White House Rolls Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling 67 packages of Ham on White House Rolls because they may have contacted equipment used to process country ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Ham on White House Rolls 12CT, NET WT 26.9 OZ (1.68lb/762g) UPC 72251525154 ,
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0613-2019·2018-11-21

    Ukrop's Honey Ham and Turkey Rolls Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling Honey Ham & Turkey on White House Rolls because they may have contacted equipment used for a Listeria recall.

    Product
    Ukrop's Honey Ham & Turkey on White House Rolls 4CT, NET WT 11 OZ (311g), UPC 72251525071
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0571-2019·2018-11-21

    Working Cow Strawberry Ice Cream Recalled for Listeria Risk

    Working Cow Homemade Inc. is recalling 76 tubs of JY Strawberry Ice Cream due to potential Listeria monocytogenes contamination.

    Product
    JY Strawberry Ice Cream, 3 gallons
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0244-2019·2018-11-21

    Teva Recalls Alprostadil Injection Due to Impurity Testing Failures

    Teva Pharmaceuticals is recalling Alprostadil Injection vials because routine stability testing revealed out-of-specification impurities.

    Product
    Alprostadil Injection USP 500 micrograms/mL 1 mL single use vial, 5 vials per carton, Rx only, TEVA Pharmaceuticals USA, Inc., North Wales, PA --- NDC 0703-1501-02
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0567-2019·2018-11-21

    Working Cow Homemade Inc. Recalls JY Chocolate Cookies Ice Cream

    Working Cow Homemade Inc. is recalling 84 tubs of JY Chocolate Cookies Ice Cream due to potential Listeria monocytogenes contamination.

    Product
    JY Chocolate Cookies Ice Cream, 3 gallons
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·18V823000·2018-11-20

    Grand Design Recalls 2019 Imagine Trailers Due to Bearing Defect

    Grand Design is recalling 2019 Imagine recreational trailers because inner hub bearings may overheat and fail, increasing crash risk.

    Product
    GRAND DESIGN — GRAND DESIGN IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·116-2018·2018-11-20

    Long Phung Recalls Pork Products Due to Possible Listeria Contamination

    Long Phung Food Products is recalling ready-to-eat pork products due to possible Listeria monocytogenes contamination linked to four confirmed illnesses.

    Product
    165368 C. Corporation — 165368 C. Corporation Recalls Pork Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V819000·2018-11-20

    Heartland Recalls 2019 Trailers Due to Bearing Grease Defect

    Heartland is recalling 2019 Pioneer and Prowler trailers because inner hub bearings may overheat and fail, increasing crash risk.

    Product
    HEARTLAND — HEARTLAND PIONEER, PROWLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V821000·2018-11-20

    Navistar Recalls 2019-2020 IC Bus CE School Buses for Brake Line Defect

    Navistar is recalling 187 IC Bus CE school buses from 2019-2020 because an improperly routed brake air line may kink, causing the vehicle to pull right or disabling anti-lock brakes.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19036·2018-11-20

    Seabreeze Recalls Smart Thermaflo Bathroom Heater Fans Due to Fire Hazard

    Seabreeze International is recalling Smart Thermaflo Bathroom Heater Fans because the safety cutoff can fail, allowing the unit to overheat and catch fire.

    Product
    Smart Thermaflo Bathroom Heater Fans with nightlight
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V818000·2018-11-19

    Audi Recalls Q5 and Q7 Models for Fuel Pump Flange Repair

    Volkswagen Group of America is recalling 2007-2012 Audi Q7 and 2009-2012 Audi Q5 vehicles to replace fuel pump flanges and install butyl tape to prevent fuel leaks and fire risk.

    Product
    AUDI — AUDI Q5, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·114-2018·2018-11-17

    Swift Beef Company Recalls Ground Beef Due to E. coli O157:H7

    Swift Beef Company is recalling approximately 99,260 pounds of raw ground beef products that may be contaminated with E. coli O157:H7. The products were distributed in California, Nevada, Oregon, Utah, and Washington.

    Product
    Swift Beef Company — Swift Beef Company Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·18V815000·2018-11-16

    Autocar Recalls 2019 Xpeditor Vehicles Due to Steering Bracket Defect

    Autocar is recalling 761 2019 Xpeditor vehicles because the power steering assist cylinder bracket may not be properly secured, potentially causing a loss of steering ability.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V813000·2018-11-16

    ARBOC Transit Bus Recall for Foldaway Seat Locking Defect

    ARBOC is recalling 2015-2018 Spirit of Freedom, Mobility, and Independence buses because foldaway seat cushions may not stay locked during a crash.

    Product
    ARBOC — ARBOC, ARBOC SPECIALTY VEHICLES SPIRIT OF INDEPENDENCE, SPIRIT OF MOBILITY, SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19717·2018-11-15

    RH Recalls Metal-Wrapped Coffee Tables Due to Lead Exposure Risk

    Restoration Hardware is recalling specific metal-wrapped coffee tables because the metal tops may contain lead, posing a health risk to children.

    Product
    Metal-wrapped coffee tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V810000·2018-11-15

    Mack Trucks Recalls 2019 Models Due to Tire Air Loss Risk

    Mack is recalling 818 2019 LR, Granite, and TerraPro trucks because specific Bridgestone tires may lose air rapidly, increasing crash risk.

    Product
    MACK — MACK LR, GRANITE (GR), TE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0252-2019·2018-11-14

    Silver Star Brands Recalls Native Remedies HypoSlim Oral Spray Due to Microbial Contamination

    Silver Star Brands is recalling 95 bottles of Native Remedies HypoSlim Oral Spray due to microbial contamination. The product was distributed nationwide in the US.

    Product
    Native Remedies HypoSlim Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-275-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0233-2019·2018-11-14

    Qualgen Recalls Testosterone Pellets Due to Sterility Assurance Concerns

    Qualgen, LLC is recalling specific lots of Testosterone 200mg pellets nationwide due to a lack of assurance of sterility.

    Product
    Testosterone 200mg pellet, 1 count (NDC 69761-120-01), 6 count (NDC 69761-120-06), 12 count (NDC 69761-120-12), and 30 count (NDC 69761-120-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0225-2019·2018-11-14

    Qualgen Recalls Estradiol Pellets Due to Lack of Sterility Assurance

    Qualgen, LLC is recalling Estradiol 10mg pellets nationwide due to a lack of assurance of sterility. The affected lots have specific expiration dates.

    Product
    Estradiol 10mg pellet, 1 count (NDC 69761-010-01), 6 count (NDC 69761-010-06), 12 count (NDC 69761-010-12), and 30 count (NDC 69761-010-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0237-2019·2018-11-14

    Qualgen Recalls Testosterone Pellets Due to Sterility Concerns

    Qualgen, LLC is recalling specific lots of Testosterone 87.5mg pellets nationwide due to a lack of assurance of sterility.

    Product
    Testosterone 87.5mg pellet, 1 count (NDC 69761-187-01), 6 count (NDC 69761-187-06), 12 count (NDC 69761-187-12), and 30 count (NDC 69761-187-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide