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.

1–25 of 84

  • HighNHTSA·26V381000·2026-06-10

    Denago EV Recalls Multiple Models for Missing Pedestrian Warning Sounds

    Denago EV is recalling 2024-2026 electric vehicles that may fail to emit pedestrian warning sounds, increasing the risk of crashes.

    Product
    DENAGO EV — DENAGO EV NOMAD XL, ROVER XL, ROVER XL6, ROVER XXL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V099000·2026-02-20

    Mercedes-Benz eSprinter Recalled for Insufficient Pedestrian Warning Sounds

    Daimler Vans USA is recalling 2025 Mercedes-Benz eSprinter vehicles because they fail to make sufficient pedestrian warning sounds when in reverse, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ESPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25C005000·2025-04-09

    Chicco Recalls MyFit Zip Air Harness and Booster Child Seats

    Chicco is recalling specific MyFit Zip Air Harness and Booster child seats because they may allow excessive chest movement in a crash, increasing injury risk.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2102-2024·2024-05-29

    Wolf Medical 3 mL Syringes Recalled for Out-of-Specification Manufacturing

    Jiangsu Shenli Medical is recalling 777,400 Wolf Medical 3 mL syringes (Model SYR03L) manufactured outside FDA clearance scope. Users should discontinue use of affected lot codes.

    Product
    Brand Name: Wolf Medical Product Name: 3 mL (cc) Luer Lock STERILE LATEX FREE NON PYROGENIC Model/Catalog Number: SYR03L Product Description: NON-Sterile syringes without needles for single use Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24E039000·2024-05-23

    Nexxpro Recalls NEXX X.G10 Helmets for Inadequate Impact Protection

    Nexxpro is recalling NEXX X.G10 helmets in sizes M and S because they may lack a required carbon layer, failing to provide adequate protection in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23E004000·2023-01-13

    Comoto Recalls Bilt Vertex Helmets for Safety Standard Non-Compliance

    Comoto Holdings is recalling specific Bilt Vertex motorcycle helmets because they may lack proper retention and penetration protection, increasing crash injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22E089000·2022-10-18

    Comoto Recalls Youth Helmets for Inadequate Impact Protection

    Comoto is recalling specific Bilt Grommet Youth helmets that may not adequately protect the wearer during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V698000·2022-09-19

    Prevost Recalls X3-45 Commuter Motorcoaches Due to Incorrect Seat Belt Type

    Prevost is recalling 2021-2023 X3-45 Commuter motorcoaches because the driver's seat has a Type 1 seat belt instead of the required Type 2, which may not adequately protect the driver in a crash.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V417000·2022-06-13

    Utilimaster Walk-In Van Recall for Incorrectly Installed Passenger Headrest

    Shyft Group is recalling 2021-2022 Utilimaster Walk-In Vans because the passenger-side jump seat headrest may be installed incorrectly, increasing injury risk in a crash.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E044000·2022-05-26

    Milwaukee Performance Helmets Recalled for Safety Standard Non-Compliance

    Milwaukee Performance Helmets is recalling specific models that fail to meet federal safety standards due to potential defects in retention, protection, and labeling.

    Product
    EQUIPMENT:OTHER:LABELS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22E006000·2022-02-03

    Nexxpro Recalls X.R2 Motorcycle Helmets Due to Impact Protection Defect

    Nexxpro is recalling specific X.R2 motorcycle helmets because they may not adequately protect the wearer in a crash. Owners will receive free replacements.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1483-2021·2021-04-28

    Welch Allyn ELI 380 Electrocardiograph Recalled for IEC 60601-2-27 Non-Compliance

    Welch Allyn Inc Mortara is recalling 27 ELI 380 Electrocardiographs because they do not meet IEC 60601-2-27 requirements as labeled.

    Product
    ELI 380 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version 1.5.1 - Product Usage: indicated for use on adult and pediatric populations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1172-2021·2021-03-10

    Barco Diagnostic Radiology Display Recalled for Lack of DICOM Compliance

    Barco N.V. is recalling MDNC-3421 diagnostic radiology displays because they were shipped without being DICOM-compliant. These units will not pass required acceptance tests.

    Product
    Barco MDNC-3421 DISPLAY, DIAGNOSTIC RADIOLOGY
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1134-2021·2021-02-24

    SenTec Digital Monitor Recalled for Missing Isolation Transformer Requirement

    SenTec AG is recalling 15 SenTec Digital Monitors because they require an isolation transformer in home care settings to meet safety standards.

    Product
    SenTec Digital Monitor, Model SDM, is a portable stand-alone patient monitor indicated for continuous, noninvasive patient monitoring of carbon dioxide partial pressure (PCo2), oxygen partial pressure (POs), functional oxygen saturation (PsO2), and pulse rate (PR), using either a
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0443-2021·2020-11-18

    Maquet BMU 40 Blood Monitoring Units Recalled for Electrical Safety Non-Compliance

    Maquet Cardiovascular is recalling 51 Blood Monitoring Units (BMU 40) because the printed circuit boards do not meet IEC electrical safety standards for creepage distance.

    Product
    Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during cardiopulmonary bypass (CPB) or similar procedures with extracorporeal circulation, which require continuous monitoring of the arterial and/or venous blood parameters: parti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20E082000·2020-10-27

    Leather on Wheels Recalls Polo Helmets for Impact Protection Defect

    Leather on Wheels is recalling Polo model helmets because they may not adequately reduce impact force, increasing the risk of injury in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide