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.

12951–12975 of 29186

  • SevereFDA (Drugs)·D-0384-2019·2019-01-30

    Recall of Curaplex Epi Safe Kits Due to Incorrect Epinephrine Instructions

    Bound Tree Medical is recalling Curaplex Epi Safe Kits because the instructions recommend an unapproved epinephrine dosage for young children.

    Product
    curaplex Epi Safe Kit, 8600-01101, contains:" 1ml Vial of Epinephrine " 1 Epi-Safe Syringe " 1 Safety Needle " 2 Alcohol Prep Pads " 1 Adhesive Dressing " 1 Insert, Rx Only. Distributed by Sarnova HC, LLC s family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2019·2019-01-29

    Tyson Recalls Chicken Nuggets Due to Possible Rubber Contamination

    Tyson Foods is recalling approximately 36,420 pounds of chicken nuggets that may contain rubber. Consumers should not eat the product and should discard it or return it to the store.

    Product
    Tyson Foods, Inc. — Tyson Foods, Inc. Recalls Chicken Nugget Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V061000·2019-01-29

    Proterra Recalls 2015-2018 Catalyst Buses for Air Brake Moisture Risk

    Proterra is recalling 2015-2018 Catalyst 40 transit buses because missing air brake components may allow moisture buildup, potentially leading to brake failure.

    Product
    PROTERRA — PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V060000·2019-01-29

    Honda Recalls Acura and Honda Vehicles for Fuel Pump Defect

    Honda is recalling 2015-2019 Acura and Honda vehicles because fuel pump particulates may cause engine stalls, increasing crash risk.

    Product
    ACURA — ACURA, HONDA MDX, ACCORD, TLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V059000·2019-01-28

    Gillig Recalls 2016-2018 Low Floor Buses for Steering Defect

    Gillig is recalling 2016-2018 Low Floor buses because a steering draglink ball stud may not be properly tightened, increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V058000·2019-01-28

    Keystone Montana Recalled for Kitchen Slide Bolt Tire Contact Risk

    Keystone RV is recalling 2019 Montana trailers because a kitchen slide adjustment bolt may contact the tire, potentially causing tire failure and increasing crash risk.

    Product
    KEYSTONE — KEYSTONE MONTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V055000·2019-01-28

    Stoughton Recalls 2016-2019 DVW Trailers Due to Cracking Hitch Points

    Stoughton is recalling 2016-2019 DVW trailers because the forward attachment points for the pintle mounting assembly may crack, potentially causing the trailer to detach from the tow vehicle.

    Product
    STOUGHTON — STOUGHTON DVW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V020000·2019-01-24

    Ram 1500 Recall: Improperly Secured Battery Ground Fastener

    Chrysler is recalling 2019 Ram 1500 vehicles because an improperly secured battery ground fastener may cause loss of power steering assist, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0370-2019·2019-01-23

    Aurobindo Recalls Valsartan Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling Valsartan tablets because FDA testing found N-nitrosodimethylamine (NDEA) above the acceptable daily intake level.

    Product
    VALSARTAN — VALSARTAN (VALSARTAN)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0363-2019·2019-01-23

    Aurobindo Recalls Amlodipine and Valsartan Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling Amlodipine and Valsartan tablets because FDA labs found N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    AMLODIPINE AND VALSARTAN — AMLODIPINE AND VALSARTAN (AMLODIPINE AND VALSARTAN)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0365-2019·2019-01-23

    Aurobindo Recalls Valsartan and Hydrochlorothiazide Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because FDA labs confirmed the presence of the impurity N-nitrosodimethylamine (NDEA) above the interim acceptable daily intake level.

    Product
    VALSARTAN AND HYDROCHLOROTHIAZIDE — VALSARTAN AND HYDROCHLOROTHIAZIDE (VALSARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·19V049000·2019-01-23

    Spartan K1 Motor Home Chassis Recalled for Brake Component Defect

    Spartan is recalling 2019-2020 K1 motor home chassis because missing or improper cotter pins may cause brake actuator rods to detach, increasing stopping distance.

    Product
    SPARTAN — SPARTAN K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0366-2019·2019-01-23

    Aurobindo Recalls Valsartan and Hydrochlorothiazide Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    VALSARTAN AND HYDROCHLOROTHIAZIDE — VALSARTAN AND HYDROCHLOROTHIAZIDE (VALSARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0369-2019·2019-01-23

    Aurobindo Recalls Valsartan and Hydrochlorothiazide Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above the acceptable daily intake level.

    Product
    VALSARTAN AND HYDROCHLOROTHIAZIDE — VALSARTAN AND HYDROCHLOROTHIAZIDE (VALSARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0362-2019·2019-01-23

    Aurobindo Recalls Amlodipine and Valsartan Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling specific lots of Amlodipine and Valsartan tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    AMLODIPINE AND VALSARTAN — AMLODIPINE AND VALSARTAN (AMLODIPINE AND VALSARTAN)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0364-2019·2019-01-23

    Aurobindo Recalls Amlodipine and Valsartan Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling Amlodipine and Valsartan tablets because FDA testing found the impurity NDEA above acceptable daily intake levels.

    Product
    AMLODIPINE AND VALSARTAN — AMLODIPINE AND VALSARTAN (AMLODIPINE AND VALSARTAN)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0368-2019·2019-01-23

    Aurobindo Recalls Valsartan and Hydrochlorothiazide Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    VALSARTAN AND HYDROCHLOROTHIAZIDE — VALSARTAN AND HYDROCHLOROTHIAZIDE (VALSARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0361-2019·2019-01-23

    Aurobindo Recalls Amlodipine and Valsartan Tablets Due to NDEA Impurity

    Aurobindo Pharma USA is recalling Amlodipine and Valsartan tablets because FDA testing found NDEA impurity levels above the acceptable daily intake.

    Product
    AMLODIPINE AND VALSARTAN — AMLODIPINE AND VALSARTAN (AMLODIPINE AND VALSARTAN)
    Category
    Drug
    Distribution
    0 states
  • SevereUSDA FSIS·006-2019·2019-01-23

    Stino Da Napoli Recalls Meat Products Produced Without Federal Inspection

    Stino Da Napoli is recalling approximately 11,392 pounds of meat products produced without federal inspection. The products were distributed to retail stores in Ohio.

    Product
    Stino Da Napoli — Stino Da Napoli Recalls Various Meat Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0367-2019·2019-01-23

    Aurobindo Recalls Valsartan and Hydrochlorothiazide Tablets Due to NDEA Impurity

    Aurobindo Pharma USA Inc. is recalling Valsartan and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    VALSARTAN AND HYDROCHLOROTHIAZIDE — VALSARTAN AND HYDROCHLOROTHIAZIDE (VALSARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·19V048000·2019-01-22

    Forest River Recalls 2017-2019 Motorhomes Due to Fire Risk

    Forest River is recalling 2017-2019 Glaval Entourage and Berkshire Coach Ultra motorhomes because a block heater cable defect may cause a fire.

    Product
    GLAVAL BUS — GLAVAL BUS, FOREST RIVER ENTOURAGE, BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·003-2019·2019-01-18

    Johnsonville Recalls Raw Pork Patties Due to Black Rubber Contamination

    Johnsonville is recalling raw ground pork patties potentially contaminated with black rubber. Consumers should discard or return the affected products.

    Product
    Johnsonville, LLC — Johnsonville, LLC Recalls Raw Ground Frozen Cheddar Cheese and Bacon Flavored Pork Patty Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide