The Recall Desk

Hazard

Inadequate Weld recalls

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

What the numbers show

Total
4
Critical
2
Severe
0
Most recent
2025-11-19

Of the 4 inadequate weld recalls we have scored against our rubric, 2 (50%) 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 inadequate weld 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.

1–4 of 4

  • HighFDA (Devices)·Z-0460-2026·2025-11-19

    Urodynamics tables recalled over an inadequate weld on the backrest bracket

    Sonesta Medical is recalling 10 Sonesta 6210 video urodynamics procedure tables because an inadequate weld on the backrest bracket can result in the backrest dropping.

    Product
    Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software Version: N/A Product Description: Sonesta 6210 - Procedure table designed for full fluoroscopic imaging of the urinary tract during video Urodynamics procedures. Component: N/A
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-0374-2026·2025-11-12

    Cranial perforators recalled as inadequate weld recall expands to smaller sizes

    Integra LifeSciences is recalling 5,109 CODMAN Disposable Perforators, 9mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.

    Product
    CODMAN Disposable Perforator 9mm. Cranial Perforator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0373-2026·2025-11-12

    Eleven millimetre cranial perforators recalled over inadequate welds

    Integra LifeSciences is recalling 16,251 CODMAN Disposable Perforators, 11mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.

    Product
    CODMAN Disposable Perforator 11mm. Cranial Perforator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1901-2020·2020-05-13

    Delfi VariFit Contour Cuffs Recalled for Inadequate Weld

    Delfi Medical Innovations is recalling 59 units of VariFit Contour Cuffs due to a manufacturing defect that may cause the cuff to leak.

    Product
    Delfi Medical Innovations, VariFit Contour Cuffs, single use adult thigh cuff, single port, single bladder, REF 9-9300-003. Rx Only, Sterile
    Category
    Medical Device
    Distribution
    1 state