The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. 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.

10351–10375 of 29158

  • SevereFDA (Drugs)·D-0639-2020·2020-01-15

    Glenmark Recalls Ranitidine Tablets Due to NDMA Impurity

    Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 150 mg because the product contains the NDMA impurity.

    Product
    Glenmark Ranitidine Tablets USP 150 mg Rx Only 60 Tablets Manufactured by: Glenmark Pharmaceuticals Ltd. Colvale-Bandez, Goa 403513, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ NDC 68462-248-60
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-0483-2020·2020-01-15

    Nestle Toll House Turtle Cookie Bars Recalled for Rubber Pieces

    Nestle Toll House Ultimate Turtle Delight Cookie Bars are being recalled due to the potential presence of food-grade rubber pieces.

    Product
    Nestle Toll House Ultimate Turtle Delight Cookie Bar (16oz), UPC 050000009282
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0495-2020·2020-01-15

    Reichel Foods Recalls Pro2Snax Snack Trays Due to Listeria Contamination

    Reichel Foods Inc. is recalling Pro2Snax To The Max snack trays due to Listeria monocytogenes contamination. The affected products were distributed nationwide.

    Product
    Pro2Snax To The Max snack tray containing Sliced Apples, Hard Boiled Egg, Mild Cheddar Cheese, and Dried Cranberries & Cashews. Item # 1-4555-6. Net Wt. 7.35 oz (208g) UPC 6 49632-00149 0 Keep Refrigerated.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0645-2020·2020-01-15

    AAA Pharmaceutical Recalls Ranitidine Tablets Due to NDMA Impurity

    AAA Pharmaceutical is recalling Ranitidine 150 mg tablets because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    Ranitidine 150 mg tablets, 24 count bottles, NDC 37808-196-01.
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·20V014000·2020-01-15

    Triumph Recalls 2019-2020 Speed Twin Motorcycles for Gear Shift Defect

    Triumph is recalling 2019-2020 Speed Twin motorcycles because the gear shift lever linkage may separate, potentially preventing gear changes and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH SPEED TWIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0643-2020·2020-01-15

    Glenmark Recalls Ranitidine Tablets Due to NDMA Impurity

    Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 300 mg because the FDA detected the NDMA impurity in the product.

    Product
    Glenmark Ranitidine Tablets USP 300 mg Rx Only 250 Tablets Manufactured by: Glenmark Pharmaceuticals Ltd. Colvale-Bandez, Goa 403513, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ NDC 68462-249-20
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0648-2020·2020-01-15

    Appco Pharma Recalls Ranitidine Capsules Due to NDMA Impurity

    Appco Pharma LLC is recalling Ranitidine Capsules 300 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    Ranitidine Capsules 300 mg, 30 count bottles. Rx only, Manufactured by: Appco Pharma LLC, Piscataway, NJ 08854, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN 56623, NDC 62559-691-30.
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0641-2020·2020-01-15

    Glenmark Recalls Ranitidine Tablets Due to NDMA Impurity

    Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 300 mg because of the presence of the NDMA impurity.

    Product
    Glenmark Ranitidine Tablets USP 300 mg Rx Only 30 Tablets Manufactured by: Glenmark Pharmaceuticals Ltd. Colvale-Bandez, Goa 403513, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ NDC 68462-249-30
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0642-2020·2020-01-15

    Glenmark Recalls Ranitidine Tablets Due to NDMA Impurity

    Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 300 mg because the FDA detected the NDMA impurity in the product.

    Product
    Glenmark Ranitidine Tablets USP 300 mg Rx Only 100 Tablets Manufactured by: Glenmark Pharmaceuticals Ltd. Colvale-Bandez, Goa 403513, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ NDC 68462-249-01
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·20V017000·2020-01-15

    BMW Recalls Vehicles for Driver Air Bag Inflator Explosion Risk

    BMW is recalling specific 2006-2015 models because driver air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    BMW — BMW 330I, 330XI, 128I, 1 SERIES M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0462-2020·2020-01-15

    Sym-Pac Recalls Frozen Yellowfin Tuna Steaks Due to Histamine Levels

    Sym-Pac International Inc is recalling 2,000 cases of frozen Yellowfin Tuna Round Steaks after customer reports of illness and high histamine levels were identified.

    Product
    Tidal Seafood Yellowfin Tuna Round Steaks; Frozen Thunnus Albacares; Net Wt.: 20 lbs. 6-8 oz. individually vacuumed packed steaks distributed Globally by: Global Protein Group, Irvine, CA
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0640-2020·2020-01-15

    Glenmark Recalls Ranitidine Tablets Due to NDMA Impurity

    Glenmark Pharmaceuticals is recalling 217,956 bottles of Ranitidine Tablets USP 150 mg nationwide because the product contains the NDMA impurity.

    Product
    Glenmark Ranitidine Tablets USP 150 mg Rx Only 100 Tablets Manufactured by: Glenmark Pharmaceuticals Ltd. Colvale-Bandez, Goa 403513, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ NDC 68462-248-01
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0780-2020·2020-01-15

    Stryker T2 Alpha Delta Strike Plate Recalled for Breakage Risk

    Stryker GmbH is recalling T2 Alpha Delta Strike Plate instruments because they can break during nail implantation or removal, potentially causing complications.

    Product
    Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of nails through the Targeting Device Catalog Number: 2351-0050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0649-2020·2020-01-15

    Appco Pharma Recalls Ranitidine Capsules Due to NDMA Impurity

    Appco Pharma LLC is recalling specific lots of Ranitidine Capsules 150 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    Ranitidine Capsules 150 mg, (a) 60 count bottles (NDC 62559-690-60) , (b) 500 count bottles (NDC 62559-690-05), Rx only, Manufactured by: Appco Pharma LLC, Piscataway, NJ 08854, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN 56623.
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·20V016000·2020-01-15

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

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

    Product
    BMW — BMW X5, X6, X6 ACTIVEHYBRID SAC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V019000·2020-01-15

    Winnebago Recalls 2020 Adventurer Motorhomes Due to Fire Risk

    Winnebago is recalling 2020 Adventurer motorhomes because a heat coil may fail to disengage, increasing the risk of a fire.

    Product
    WINNEBAGO — WINNEBAGO ADVENTURER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0646-2020·2020-01-15

    AAA Pharmaceutical Recalls Ranitidine Tablets Due to NDMA Impurity

    AAA Pharmaceutical is recalling specific lots of Ranitidine 150 mg tablets because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    Ranitidine 150 mg tablets, 130 count bottles, NDC 37808-196-04.
    Category
    Drug
    Distribution
    0 states
  • SevereUSDA FSIS·002-2020·2020-01-10

    Culinary International Recalls Chicken Burritos Due to Undeclared Egg Allergen

    Culinary International is recalling approximately 626 pounds of frozen chicken burritos that actually contain eggs, an undeclared allergen. No illnesses have been reported.

    Product
    Ruiz Food Products, Inc. — Culinary International, LLC Recalls Chicken Burrito Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V011000·2020-01-10

    GM Recalls 2007-2008 Trucks for Air Bag Inflator Defect

    General Motors is recalling 2007-2008 Chevrolet Silverado and GMC Sierra trucks because front passenger air bag inflators may explode.

    Product
    GMC — GMC, CHEVROLET SIERRA 2500, SIERRA 3500, SILVERADO 2500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V010000·2020-01-10

    Genuine Scooter Recalls 2020 Royal Alloy GT150 Due to Brake Rotor Defect

    Genuine Scooters is recalling 2020 Royal Alloy GT150 scooters because the front brake rotor may become uncentered, potentially causing a loss of braking and increasing crash risk.

    Product
    GENUINE SCOOTER — GENUINE SCOOTER ROYAL ALLOY
    Category
    Vehicle
    Distribution
    Distributed nationwide