The Recall Desk

Hazard

Non Compliance recalls

84 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
84
Critical
0
Severe
3
Most recent
2026-06-10

Of the 84 non compliance recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (4%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all non compliance recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

26–50 of 84

  • HighCPSC·20771·2020-08-27

    Morpher Flat-Folding Bicycle Helmets Recalled for Head Injury Risk

    CPSC warns consumers to stop using and dispose of Morpher flat-folding bicycle helmets because they do not meet federal safety standards, posing a risk of head injury.

    Product
    Morpher flat-folding bicycle helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V102000·2020-02-21

    CHTC HT-35 and HT-45 Buses Recalled for Non-Compliant Wheelchair Lifts

    CHTC Bus Group is recalling 2016-2018 HT-35 and HT-45 buses because their wheelchair platform lifts failed to complete the required compliance certification process.

    Product
    CHTC BUS — CHTC BUS HT-45, HT-35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V488000·2018-07-23

    Karma Revero Recalled for Non-Compliant Driver Side Rearview Mirror Glass

    Karma Automotive is recalling 2018 Revero vehicles because the driver's side exterior rearview mirror may use convex glass instead of flat glass, failing federal safety standards.

    Product
    KARMA — KARMA REVERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V377000·2018-06-06

    Spartan Recalls Utilimaster Vans for Missing Seat Belt Retractors

    Spartan Motors is recalling 1991-2018 Utilimaster Aeromaster and Walk-In Vans because front seat belts lack required retractors, increasing crash injury risk.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN, AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E014000·2017-03-07

    H&H Sports Protection Recalls TORC T-55 V2 Motorcycle Helmets

    H&H Sports Protection is recalling TORC T-55 V2 half helmets because they may not adequately protect the wearer or stay secured during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E081000·2016-10-28

    Vega Motorcycle Helmets Recalled for Failing Federal Safety Standards

    Vega Helmet Corporation is recalling specific XTA and XTA Touring half helmets because they may not adequately protect the wearer's head in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V615000·2016-08-24

    Hyundai Recalls 2016 Sonata Vehicles Due to Driver Air Bag Defect

    Hyundai is recalling specific 2016 Sonata vehicles because the driver-side frontal air bag may not adequately protect the driver's neck in a crash.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1452-2016·2016-08-10

    Let's Talk Health Recalls Unapproved Oxygen Nasal Wash Solution

    Let's Talk Health is recalling 417 bottles of Oxygen Nasal Wash because the product was marketed without FDA approval and does not comply with nasal decongestant monograph requirements.

    Product
    Oxygen Nasal Wash (purified water, xylitol, stabilized oxygen, sodium chloride) solution, .75 oz (22mL) bottle, Distributed by: Let's Talk Health, Chula Vista, CA 91914.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·16E068000·2016-08-05

    WSB Recalls WSB777 Half Helmets for Insufficient Crash Protection

    WSB Inc is recalling WSB777 half helmets manufactured in May 2015 because they may lack required labeling and fail to provide adequate head protection in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16C006000·2016-07-05

    Combi Coccoro Convertible Child Restraints Recalled for Crash Injury Risk

    Combi is recalling Coccoro Convertible Child Restraints because excessive force may be transmitted to the occupant in a crash if the seat is forward-facing and secured only with a lap belt.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E048000·2016-05-23

    Tucker Rocky Recalls Speed and Strength SS2200 Motorcycle Helmets

    Tucker Rocky is recalling Speed and Strength SS2200 motorcycle helmets that failed federal penetration testing. Owners should contact the company to receive a free replacement.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0843-2016·2016-05-18

    Sesderma Salises Acne Gel Recalled for cGMP Deviations

    Sesderma is recalling Salises Facial Moisturizing Acne Treatment Gel due to cGMP deviations. The product does not comply with current Good Manufacturing Practice requirements.

    Product
    Salises Facial Moisturizing Acne Treatment Gel, (salicylic acid 1.5%), 1.7 fl. oz (50 mL) bottle, over the counter, Manufactured by Sesderma S.L., Valencia, Spain --- NDC 63181-0016
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1231-2016·2016-04-13

    GE Cabinet X-ray Systems Recalled for Non-Compliance with FDA Standards

    GE Inspection Technologies is recalling 55 cabinet x-ray systems used for industrial quality control because they may not fully comply with FDA performance standards.

    Product
    GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
    Category
    Medical Device
    Distribution
    24 states