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.

18701–18725 of 32108

  • SevereFDA (Drugs)·D-0146-2017·2016-11-30

    VistaPharm Recalls Lactulose Solution Due to Bacterial Contamination

    VistaPharm is recalling Lactulose Solution, USP, 10 g/15 mL, because bulk solution tested positive for Burkholderia cepacia bacteria.

    Product
    Lactulose Solution, USP, 10 g/15 mL, 15 mL unit dose cups (NDC 66689-039-01), packaged in 15 mL x 50 unit dose cups per case (NDC 66689-039-50), Rx only, Manufactured by VistaPharm, Inc., Largo, FL 33771.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0528-2017·2016-11-30

    Heartland Entrees Dumplings and Broth Recalled for Undeclared Milk

    St Clair Foods, Inc. is recalling Heartland Entrees Dumplings and Broth because the product contains undeclared milk.

    Product
    HEARTLAND ENTREES DUMPLINGS AND BROTH, Product Code 856140, NET WEIGHT: (320 ozs)(9.09 kg)(4-5 Lbs), KEEP FROZEN
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·16V857000·2016-11-29

    Van Hool Motorcoaches Recalled for Steering Knuckle Carrier Cracking

    Van Hool is recalling specific motorcoaches because front steering knuckle carriers may crack, potentially causing a wheel to separate and increasing crash risk.

    Product
    VAN HOOL — VAN HOOL TD925, C2045, T2140, T2145
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17039·2016-11-29

    Gree Recalls 2.5 Million Dehumidifiers Due to Fire and Burn Hazards

    Gree Electric Appliances is recalling approximately 2.5 million dehumidifiers sold under various brands because they can overheat and catch fire, posing serious fire and burn hazards.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V855000·2016-11-28

    Autocar Recalls 2013-2017 Xpeditor Vehicles for Engine Stall Risk

    Autocar is recalling 2013-2017 Xpeditor vehicles because fuse box vibration may cause the ignition relay to open, leading to an engine stall and increased crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V853000·2016-11-28

    Mercedes-Benz Sprinter Recall for Defective Left Seat Adjusters

    Midwest Automotive Designs is recalling 2016 Mercedes-Benz Sprinter 2500 and 3500 vans because certain left seat adjusters may allow seats to move during a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V852000·2016-11-28

    Autocar Recalls Xpeditor Vehicles for Hybrid Drive Unit Bolt Defect

    Autocar is recalling 2012-2016 Xpeditor vehicles because hybrid power drive unit bolts may not be tightened properly, risking detachment and crashes.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V856000·2016-11-28

    Maserati Recalls 2017 Quattroporte and Ghibli for Rear Differential Defect

    Maserati is recalling 326 model year 2017 Quattroporte and Ghibli vehicles because a loose rear differential pinion nut may cause the rear wheels to lock up, increasing crash risk.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V854000·2016-11-28

    KTM Recalls 2013-2016 Adventure Motorcycles for Brake Line Melting Risk

    KTM is recalling specific 2013-2016 Adventure and Super Adventure motorcycles because a fraying wiring harness can melt the brake line, potentially causing brake failure.

    Product
    KTM — KTM 1190 ADVENTURE, 1190 ADVENTURE R, 1290 SUPER ADVENTURE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V850000·2016-11-23

    Kalmar Recalls 2014-2016 Ottawa T2 Vehicles for Fire Risk

    Kalmar is recalling 798 model year 2014-2016 Ottawa T2 vehicles because an overloaded ground circuit may increase the risk of a dashboard fire.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0454-2017·2016-11-23

    Turkey Hill Rocky Road Ice Cream Recalled for Unlabeled Allergens

    Turkey Hill Dairy is recalling Rocky Road ice cream because it may contain unlabeled almonds and eggs, posing a risk of severe allergic reactions.

    Product
    On Lid: Turkey Hill, Rocky Road, 48 FL. OZ.. In small letters at the top of the lid reads: "Dutch Chocolate ice cream swirled with whipped marshmallow and butter-roasted almonds" On body of Tub: Turkey Hill Rocky Road, 48 FL. OZ. On bottom of Tub: Sell By May 23, 2017…
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Drugs)·D-0141-2017·2016-11-23

    Sandoz Recalls L-Cysteine Hydrochloride Injection Due to Sterility Concerns

    Sandoz Inc. is recalling L-Cysteine Hydrochloride Injection vials because an FDA inspection raised concerns that the product's sterility may be compromised.

    Product
    L-Cysteine Hydrochloride Injection, USP, 50 mg/mL, 50 mL Pharmacy Bulk Package Vials (NDC 66758-005-01), packaged in 5 x 50 mL Vials per carton(NDC 66758-005-02), Rx only, Manufactured for: Sandoz, Inc., Princeton, NJ.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0433-2017·2016-11-23

    McCain Foods Recalls Frozen Onion Rings for Undeclared Milk

    McCain Foods USA is recalling frozen onion rings sold under six private label brands because the product label does not declare milk.

    Product
    Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and Match Onion Rings, NET WT 40 OZ, packaged in plastic bags; 2) Krasdale Onion Rings, NET WT 16 OZ, packaged in plastic bags; 3) Spartan Onion Rings, NET WT 20…
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Devices)·Z-0487-2017·2016-11-23

    ICU Medical Recalls SafeSet Reservoir Kits Due to Potential Leak

    ICU Medical is recalling 205 SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.

    Product
    Cath Lab Kit For Elkhart Hosp., Item No. 46078-17 The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure into electrical currents that can be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0140-2017·2016-11-23

    Sandoz Recalls L-Cysteine Hydrochloride Injection Due to Sterility Concerns

    Sandoz Inc. is recalling L-Cysteine Hydrochloride Injection because an FDA inspection raised concerns that the product's sterility may be compromised.

    Product
    L-Cysteine Hydrochloride Injection, USP, 0.5 g/10 mL (50 mg/mL), 10 mL Single Dose Vial (NDC 66758-004-01), packaged in 10 x 10mL Vials per carton (NDC 66758-004-02), Rx only, Manufactured for: Sandoz Inc., Princeton, NJ 08540.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·114-2016·2016-11-23

    Nick's of Calvert Recalls Meatballs for Undeclared Allergens

    Nick's of Calvert is recalling 305 pounds of meatballs sold in Maryland due to missing production information and undeclared eggs and milk.

    Product
    Nick's of Calvert Recalls Meatball Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0476-2017·2016-11-23

    Prime Time International Recalls Cucumbers Due to Salmonella Risk

    Prime Time International is recalling cucumbers because they may be contaminated with Salmonella.

    Product
    PRIME TIME Cucumbers, 1 & 1/9 BUSHEL CARTON, 25kg per carton, TAG ID# 10173318, 10173319, 10173320, 10173322.
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·111-2016·2016-11-22

    Heinz Recalls Mislabeled Au Jus Gravy Containing Undeclared Allergens

    H.J. Heinz is recalling approximately 5,022 pounds of bistro au jus gravy that was incorrectly labeled as pork gravy. The product contains undeclared milk and soy allergens.

    Product
    H.J. Heinz Co. Recalls Products Incorrectly Labeled As Pork Gravy Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V840000·2016-11-21

    Maserati Recalls Ghibli and Quattroporte Vehicles for Tire Sidewall Cracks

    Maserati is recalling 1,861 Ghibli and Quattroporte vehicles because certain Pirelli tires may develop sidewall cracks, potentially causing air loss and vehicle control issues.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide