The Recall Desk

Hazard

Safety Standard Non Compliance recalls

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

What the numbers show

Total
15
Critical
0
Severe
1
Most recent
2024-04-17

Of the 15 safety standard 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 1 (7%) 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 safety standard 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.

1–15 of 15

  • HighFDA (Devices)·Z-1488-2024·2024-04-17

    Medline SwivAssist Bed Assist Bars Recalled for Safety Standard Non-Compliance

    Medline is recalling 79 Bed Assist Bars that failed to comply with federal safety standards for adult portable bed rails. The products were manufactured after the compliance deadline.

    Product
    Bed Assist Bars, labeled as follows: a) Medline SwivAssist Bar, Model Number MDS6800SWIV (case of 3), b) Medline SwivAssist Bar, Model Number MDS6800SWIVRH (individual)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24708·2023-11-02

    Murf Electric Bicycles Recalled for Fall and Injury Hazards

    Murf Electric Bikes is recalling about 9,000 electric bicycles sold from July 2017 through April 2022 because they do not meet U.S. safety standards and pose fall and injury hazards. The company has received one report of a fall with minor injury.

    Product
    Electric bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23785·2023-08-24

    Ecnup Kids Bike Helmets Recalled Due to Head Injury Risk

    Ecnup kids bike helmets sold on Amazon do not meet federal safety standards for coverage, stability, and labeling. The helmets can fail to protect the head in a crash.

    Product
    Kids bike helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23230·2023-06-22

    Hurtle Multi-Purpose Helmets Recalled Due to Risk of Head Injury

    Sound Around is recalling about 1,800 Hurtle multi-purpose children's helmets because they do not meet federal safety standards for positional stability and may fail to protect in a crash.

    Product
    Hurtle Multi-Purpose Helmet
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23747·2023-04-20

    Lelinta Multi-Purpose Kids Helmets Recalled for Head Injury Risk

    Lucky Global is recalling about 30 Lelinta Multi-Purpose Kids Helmets sold online at Walmart.com because they do not meet federal safety standards for positional stability and may fail to protect children in a crash.

    Product
    Lelinta Multi-Purpose Kids Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23730·2023-03-02

    Multi-Purpose Kids Bike Helmets Recalled for Head Injury Risk

    Ouwoer Kids Bike Helmets sold on Amazon from March to November 2022 fail to meet federal safety standards and may not protect children in a crash. About 120 units are affected; no injuries have been reported.

    Product
    Multi-Purpose Kids Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22185·2022-07-14

    Sakar International Recalls Tony Hawk Silver Helmets Due to Head Injury Risk

    Sakar International is recalling about 12,655 Tony Hawk Silver Metallic multi-purpose helmets sold at Walmart from March to June 2022. The helmets do not meet federal safety standards for positional stability and retention, and may fail to protect in a crash.

    Product
    Tony Hawk Silver Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22106·2022-03-24

    Sakar Dimensions Bluetooth Speaker Helmets Recalled for Head Injury Risk

    Sakar International is recalling about 89,000 Dimensions Bluetooth Speaker Helmets sold at Walmart because they do not meet U.S. federal safety standards for bicycle helmets and pose a risk of head injury in a fall.

    Product
    Dimensions Bluetooth Speaker Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0335-2022·2021-12-15

    OsteoMed Surgical Consoles Recalled for Electrical Safety Violations

    OsteoMed OsteoPower Power Consoles and footswitches are being recalled due to non-compliance with electrical safety standard IEC 60601. The product has shocked a patient, creating a significant electrical hazard.

    Product
    OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control Console 2 REF 450-0021-01 -Power Control Console 2 REF ECOS-450-0021-00 -OsteoMed OsteoPower Power Console 2i REF 450-0005-00 -OsteoMed D-Power Control Conso
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21193·2021-09-01

    TurboSke Kids Toddler Bike Helmets Recalled for Head Injury Risk

    SKE Outdoors is recalling about 860 TurboSke Kids Toddler Bike Helmets (size small) because they do not meet U.S. CPSC federal safety standards, posing a risk of head injury. No injuries have been reported.

    Product
    TurboSke Kids Toddler Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1484-2021·2021-04-28

    Welch Allyn Surveyor Bedside Patient Monitor Recalled for Safety Standard Non-Compliance

    Welch Allyn is recalling 213 Surveyor S12/S19 Bedside Patient Monitors because they do not meet IEC 60601-2-27 safety requirements as labeled.

    Product
    Surveyor S12/S19 Bedside Patient Monitor, 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-1482-2021·2021-04-28

    Welch Allyn ELI 280 Electrocardiograph Recalled for Safety Standard Non-Compliance

    Welch Allyn is recalling 99 ELI 280 Electrocardiographs because they do not meet IEC 60601-2-27 safety requirements as labeled.

    Product
    ELI 280 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
  • HighFDA (Devices)·Z-2870-2017·2017-09-20

    X-Laser High-Power Laser Projectors Recalled for Safety Standard Non-Compliance

    X-Laser is recalling 830 high-power laser light show projectors because they fail to meet federal performance standards when used in auto and music modes.

    Product
    X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Beam, Hawk 500 High-power laser light show projector.
    Category
    Consumer Product
    Distribution
    0 states