The Recall Desk

Hazard

De Bonding recalls

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

What the numbers show

Total
2
Critical
0
Severe
0
Most recent
2022-02-23

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

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all de bonding 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.

1–2 of 2

  • HighFDA (Devices)·Z-0644-2022·2022-02-23

    Howmedica Osteonics Medical Device Packaging Defect: Tyvek Lid De-bonding Recall

    Howmedica Osteonics is recalling medical devices because the outer Tyvek lid may separate from the package seal. This affects 32MM -4 V40 TAPER VIT HEAD devices distributed worldwide.

    Product
    32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0645-2022·2022-02-23

    Howmedica Dall Miles SM GRIP surgical device recalled for potential package de-bonding

    Howmedica is recalling the Dall Miles SM GRIP device because the outer Tyvek protective package may separate from the sealed unit. The affected batch should be inspected before use.

    Product
    Dall Miles SM GRIP AND 2 1.6MM HOMOG CBL, Catalog Number 6704-0-110
    Category
    Medical Device
    Distribution
    1 state