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.

7176–7200 of 29119

  • SevereFDA (Food)·F-0608-2022·2022-02-02

    Fresh Express Twisted Chopped Asian Caesar Salad Recalled for Listeria

    Fresh Express Inc is recalling Twisted Chopped Asian Caesar salad in 9.6oz packages due to potential Listeria monocytogenes contamination. The product was distributed to domestic and Canadian distributors.

    Product
    "Twisted Chopped Asian Caesar" (salad product) packed in 9.6oz. packages
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-0531-2022·2022-02-02

    Fresh Express Bacon & Blue Salad Recalled for Listeria Risk

    Fresh Express Inc is recalling "Bacon & Blue" salad products (10.8 oz and 10.9 oz packages) distributed across 20 U.S. states and Canada due to potential Listeria monocytogenes contamination.

    Product
    "Bacon & Blue" (salad product) packed in 10.8oz. and 10.9oz. packages
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-0567-2022·2022-02-02

    Fresh Express Leafy Romaine Salad Recalled for Listeria Contamination Risk

    Fresh Express Inc is recalling Leafy Romaine salad in 9oz. and 10oz. packages due to potential Listeria monocytogenes contamination. The product was distributed to multiple states and Canada.

    Product
    "Leafy Romaine" (salad product) packed in 9oz. and 10oz. packages
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Drugs)·D-0426-2022·2022-02-02

    Vancomycin HCl Injection Recalled for Sterility Assurance Issues

    Edge Pharma LLC is recalling Vancomycin HCl in 0.9% Sodium Chloride Injection nationwide due to lack of assurance of sterility. The affected product is a 500 mL pre-filled bag for IV injection.

    Product
    Vancomycin HCl in 0.9% Sodium Chloride Injection, 1,500 mg/500 mL, USP, Single Use Bag for IV Injection (Preservative Free), 500 mL pre-filled bag, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1458-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V053000·2022-02-02

    2021-2022 Jayco and Entegra motorhomes recalled for loose tie rod clamps

    Jayco and Entegra are recalling certain 2021-2022 Class C motorhomes with loose tie rod clamps that could lead to steering loss and increased crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA SENECA, ACCOLADE, ACCOLADE XL, SENECA PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V047000·2022-02-01

    Seagrave Recalls 2021 Capitol and Marauder Vehicles for Axle Defect

    Seagrave is recalling 2021 Capitol and Marauder vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake unexpectedly and increasing crash risk.

    Product
    SEAGRAVE — SEAGRAVE CAPITAL, MARAUDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V042000·2022-01-28

    Mercedes-Benz Recalls 2021 AMG GT Black Series for Wiring Harness Defect

    Mercedes-Benz is recalling 2021 AMG GT Black Series vehicles because an incorrectly sized front wheel speed sensor wiring harness may damage, impairing safety systems and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E005000·2022-01-28

    Samsung SDI Recalls High Voltage Battery Packs for Sudden Power Loss

    Samsung SDI is recalling specific high voltage battery packs that may fail, causing a sudden loss of drive power and increasing crash risk.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E004000·2022-01-27

    Prevost Recalls Seat Brackets That May Fail in Crashes

    Prevost is recalling certain seat brackets that may not meet strength requirements, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0377-2022·2022-01-26

    SENNA Syrup unit-dose cups recalled for microbial contamination

    Lohxa, LLC is recalling SENNA Syrup (sennosides) 8.8 mg/5 mL unit-dose cups due to microbial contamination of the non-sterile product. The recall affects Lot #AM1115S with expiration date 01/2023, distributed nationwide.

    Product
    SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0505-2022·2022-01-26

    Haifa Smoked Turbot Fish Recalled for Listeria Contamination

    D & M Smoked Fish, Inc. is recalling Haifa Smoked Turbot Cold Smoked (8 oz) because it may be contaminated with Listeria monocytogenes. The product was distributed in New York and New Jersey.

    Product
    "Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z."
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0451-2022·2022-01-26

    Medtronic HawkOne Directional Atherectomy Device Recalled for Tip Damage

    Medtronic is recalling 28,094 units of its HawkOne directional atherectomy system due to reports of catheter tip damage and detachment that can cause blood clots in blood vessels.

    Product
    Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-S and H1-S-INT, Small Vessel, 6F (2.2 mm) Recommended sheath, 0.014" (0.36 mm) Compatible guidewire. The HawkOne directional atherectomy system is intended for use in atherectomy of the peripheral vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V032000·2022-01-26

    Pierce Fire Trucks Recalled for Fuel Tube Cracking and Leak Risk

    Pierce Manufacturing is recalling 2015-2021 Enforcer, Quantum, Velocity, and Arrow XT fire trucks because fuel tubes may crack and leak high-pressure fuel, increasing fire risk.

    Product
    PIERCE — PIERCE ENFORCER, QUANTUM, VELOCITY, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0462-2022·2022-01-26

    Semglee Insulin Glargine Prefilled Pens Missing Label

    Mylan Pharmaceuticals is recalling approximately 73,175 Semglee (insulin glargine) prefilled pens nationwide because some units have a missing label. Patients should check their pens and contact their pharmacist or doctor if affected.

    Product
    Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3 mL Prefilled Pens per carton (NDC 49502-0196-75), Rx only, Manufactured in Malaysia for: Mylan Specialty L.P., Morgantown, WV, 26505.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V028000·2022-01-24

    Inland Empire Trailers Recalls 2021 Models Due to Axle Spindle Nut Issues

    Inland Empire Trailers is recalling 50 units of 2021 trailers because improperly tightened axle spindle nuts may cause overheating and loss of control.

    Product
    INLAND EMPIRE TRAILERS — INLAND EMPIRE TRAILERS CUSTOM TRAILER, UTILITY/ DUMP TRAILER, FLAT DECK TRAILER, ENCLOSED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V025000·2022-01-21

    Rosenbauer Fire Trucks Recalled for Rear Axle Drive Pinion Fracture Risk

    Rosenbauer America is recalling 127 Commander, Warrior, and Avenger vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, WARRIOR, AVENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V023000·2022-01-21

    BMW Recalls 2019-2020 K 1600 Motorcycles for Rear Suspension Defect

    BMW is recalling 2019-2020 K 1600 GT, GTL, and B motorcycles because a rear suspension link strut may be insufficiently strong, potentially affecting stability and increasing crash risk.

    Product
    BMW — BMW K 1600 GTL, K 1600 GT, K 1600 B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V019000·2022-01-20

    Spartan Fire Vehicles Recalled for Rear Axle Drive Pinion Fracture Risk

    Marion Body Works is recalling 2021-2022 Spartan Fire vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning and increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E003000·2022-01-20

    Pacific Trailer Recalls RAM A Frame Couplers Due to Welding Defect

    Pacific Trailer is recalling RAM A Frame 2 5/16" couplers because improper welding may cause the trailer to separate from the tow vehicle.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0431-2022·2022-01-19

    Dynamik Muscle Warbringer Capsules recalled for undeclared milk

    NutraCap Labs is recalling Dynamik Muscle Warbringer Capsules because the product contains undeclared milk, which poses a risk to consumers with milk allergies.

    Product
    Dynamik Muscle Warbringer Capsules 90ct Bottle UPC CODE 5 00102 92106
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0499-2022·2022-01-19

    Vyce World Nutrition Bed Burn Capsules recalled for undeclared milk

    NutraCap Labs LLC is recalling Vyce World Nutrition Bed Burn Capsules 60ct bottles because they contain undeclared milk, a common allergen that poses a risk to consumers with milk allergies.

    Product
    Vyce World Nutrition Bed Burn Capsules 60ct Bottle NO UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0401-2022·2022-01-19

    Vital Force PUREISO Whey Protein Isolate recalled for undeclared milk

    NutraCap Labs LLC is recalling Vital Force PUREISO 100% Whey Protein Isolate in Creamy Peanut Butter Vanilla flavor because the product contains undeclared milk, a common allergen.

    Product
    Vital Force PUREISO 100% WHEY PROTEIN ISOLATE CREAMY PEANUT BUTTER VANILLA NET WEIGHT: 1122 (1122.0 (39.58 OZ) Ingredients: Whey Protein Isolate, Coconut***StevioBliss Manufactured For Vital Force Rx 1580 Montgomery Hwy #14 Hoover, AL 35216 UPC 8 60006 41005 6
    Category
    Food
    Distribution
    26 states