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.

12976–13000 of 29186

  • SevereUSDA FSIS·004-2019·2019-01-18

    H & T Seafood Recalls Frozen Siluriformes Fish Products for Import Inspection Failure

    H & T Seafood, Inc. is recalling approximately 71,435 pounds of frozen Siluriformes fish products because they were not presented for import re-inspection upon entry into the United States.

    Product
    H & T Seafood, Inc. Recalls Siluriformes Products Produced without Benefit of Import Inspection
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·19V044000·2019-01-18

    Hino Recalls NJ8J Trucks for Missing Front Brake Dust Shields

    Hino is recalling 2007-2019 NJ8J trucks because missing front brake dust shields can cause the vehicle to pull left in wet conditions, increasing crash risk.

    Product
    HINO — HINO NJ8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V040000·2019-01-17

    Land Rover Recalls 2019 Models for Crankshaft Bolt Fracture Risk

    Jaguar Land Rover is recalling 2019 Range Rover and Discovery models because a crankshaft pulley bolt may fracture, causing engine failure and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER VELAR, RANGE ROVER, RANGE ROVER SPORT, DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2019·2019-01-17

    Perdue Recalls Gluten-Free Chicken Nuggets Due to Wood Contamination

    Perdue Foods is recalling approximately 68,244 pounds of SimplySmart Organics Gluten Free Chicken Nuggets due to possible wood contamination. Consumers should discard or return the product.

    Product
    Perdue Foods LLC — Perdue Foods LLC Recalls Simplysmart Organics Gluten Free Chicken Nugget Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V039000·2019-01-17

    Jaguar Recalls 2019 F-Pace, F-Type, and XJ for Crankshaft Bolt Defect

    Jaguar is recalling 2019 F-Pace, F-Type, and XJ vehicles because a defective crankshaft pulley bolt may fracture, causing engine failure and increasing crash risk.

    Product
    JAGUAR — JAGUAR F-PACE, F-TYPE, XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0352-2019·2019-01-16

    Heritage Pharmaceuticals Recalls Cidofovir Injection Due to Sterility Concerns

    Heritage Pharmaceuticals is recalling Cidofovir Injection vials due to complaints about dried powder on the outside of the bottles, which raises concerns about sterility.

    Product
    Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials, Rx only, Mfd by: Emcure Pharmaceuticals Ltd., Hinjawadi, Pune, India Mfg. for : Heritage Pharmaceuticals Inc. NDC 23155-0216-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0351-2019·2019-01-16

    Baxter Recalls Dianeal Low Calcium Dialysis Solution Due to Sterility Concerns

    Baxter Healthcare is recalling 29,370 bags of Dianeal Low Calcium peritoneal dialysis solution because confirmed customer complaints identified leaks in the tubing, compromising sterility.

    Product
    DIANEAL LOW CALCIUM WITH DEXTROSE — DIANEAL LOW CALCIUM WITH DEXTROSE (SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0357-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Rubber Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP vials because grey rubber flecks were found in the reconstituted product.

    Product
    Ceftriaxone for Injection USP, 1 g, packaged in a) one Single Use Vial (NDC 68180-633-01) and b) 10 Single Use Vials per box (NDC 68180-633-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0355-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Rubber Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 250 mg, due to the presence of grey rubber particulate matter from stoppers in reconstituted vials.

    Product
    Ceftriaxone for Injection USP, 250 mg, packaged in a) one Single Use Vial (NDC 68180-611-01) and b) 10 Single Use Vials per box (NDC 68180-611-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0356-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 500 mg, due to the presence of grey rubber particulate matter from stoppers.

    Product
    Ceftriaxone for Injection USP, 500 mg, packaged in a) one Single Use Vial (NDC 68180-622-01) and b) 10 Single Use Vials per box (NDC 68180-622-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V019000·2019-01-16

    GM Recalls 2010-2011 Chevrolet Malibu for Air Bag Inflator Defect

    General Motors is recalling 2010-2011 Chevrolet Malibu vehicles because the driver's air bag inflator may explode during a crash, potentially causing serious injury or death.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0765-2019·2019-01-16

    Adam Bros. Family Farms Cauliflower Recalled for E. coli O157:H7 Contamination

    Adam Bros. Farming, Inc. is recalling specific cases of Adam Bros. Family Farms Cauliflower due to potential E. coli O157:H7 contamination. The product was distributed in 10 states.

    Product
    Adam Bros. Family Farms Cauliflower; Sold in cases with 9, 12, 16 or 20 count cases
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·19V035000·2019-01-16

    Audi Recalls A8, A7, A6, and Q7 Models for Fuel Rail Leaks

    Audi is recalling specific 2015-2018 models because fuel rails may leak, increasing the risk of fire if an ignition source is present.

    Product
    AUDI — AUDI A8, A7, A6, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0697-2019·2019-01-16

    Swissray Medical Recalls ddRCombi Plus FP X-ray Systems Due to Lifting Column Defect

    Swissray Medical AG is recalling three ddRCombi Plus FP X-ray systems because a lifting column component may break, causing the arm to drop and potentially seriously injure patients or users.

    Product
    ddRCombi Plus FP, Model Number 8.2000.0070.0 (US Version), 8.2000.0060.0 (Europe Version) The ddRCombi Plus FP is a fully digital, multifunctional X-ray system that allows the direct digitization of X-ray information without use of cassettes or other media. It can perform all…
    Category
    Medical Device
    Distribution
    2 states
  • SevereNHTSA·19V018000·2019-01-15

    Chrysler Recalls Vehicles Due to Exploding Passenger Air Bag Inflator Risk

    Chrysler is recalling specific 2010-2016 Dodge, Chrysler, and Jeep vehicles because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    DODGE — DODGE, JEEP, CHRYSLER CHALLENGER, RAM 3500, RAM 4500, RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V015000·2019-01-14

    BMW Recalls 2000-2004 Models for Air Bag Inflator Explosion Risk

    BMW is recalling specific 2000-2004 5 Series and X5 vehicles because the air bag inflator in optional sports steering wheels may explode, posing a serious injury risk.

    Product
    BMW — BMW 540I, 525I, X5 SAV, 530I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V016000·2019-01-14

    BMW Recalls 2015 X1 Vehicles for Driver Air Bag Inflator Defect

    BMW is recalling 2015 X1 vehicles because the driver's air bag inflator may explode due to humidity, posing a risk of serious injury or death.

    Product
    BMW — BMW X1 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V017000·2019-01-14

    BMW Recalls X5 and X6 Models Due to Air Bag Inflator Defect

    BMW is recalling 2007-2014 X5 and X6 models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW X5, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V032000·2019-01-14

    Volvo Recalls 2018-2019 VNL Trucks for Clutch Assembly Defect

    Volvo is recalling 2018-2019 VNL trucks with automated manual transmissions because a clutch component may fail, causing unintended vehicle movement.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V014000·2019-01-11

    Volkswagen and Audi Recall Vehicles Due to Airbag Inflator Defect

    Volkswagen is recalling specific 2015-2017 models because the driver's airbag inflator may explode during deployment, potentially causing serious injury.

    Product
    AUDI — AUDI, VOLKSWAGEN R8 SPYDER, TT ROADSTER, CC, EOS
    Category
    Vehicle
    Distribution
    Distributed nationwide