The Recall Desk

Hazard

Improper Securing recalls

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

What the numbers show

Total
3
Critical
0
Severe
2
Most recent
2026-03-13

Of the 3 improper securing recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (67%) 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 improper securing 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.

1–3 of 3

  • HighNHTSA·26V149000·2026-03-13

    Micro Bird Recalls School Buses Due to Wheelchair Tie-Down Defect

    Micro Bird is recalling certain school buses because an installation error may prevent wheelchair tie-downs from locking, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1548-2013·2013-06-26

    Biomet Recalls Superior Approach Resection Guide Assembly Due to Slot Offset

    Biomet is recalling 17 units of the Superior Approach Resection Guide Assembly because a manufacturing defect may prevent the guide from securing properly to bone during surgery.

    Product
    Superior Approach Resection Guide Assembly. Indicated for primary, fracture, or revision total shoulder replacement for the relief of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1066-2013·2013-04-17

    Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled

    Stelkast Co is recalling 254 units of the Cross-over Acetabular Shell and Liner Hip System due to difficulty engaging and securing the liner.

    Product
    Stelkast Cross-over Acetabular Shell and Liner Hip System, Part Numbers SC3458-52, SC3474-52, SC3459-52, and SC3460-52. Intended for use in reconstruction of the articulating surface of the acetabular portion of the hip.
    Category
    Medical Device
    Distribution
    Distributed nationwide