The Recall Desk

Hazard

Peripheral Ischemia 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
2022-05-04

Of the 2 peripheral ischemia 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 peripheral ischemia 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-1016-2022·2022-05-04

    Empower Introducer Sheath Recalled for Defective Glue and Embolism Risk

    Freudenberg Medical is recalling the Empower Introducer Sheath due to defective adhesive on the catheter shaft that could cause blood clots and tissue damage.

    Product
    Empower Introducer Sheath with Hydrophilic Coating 21F x 56cm Model: 668782-100 (US)
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1017-2022·2022-05-04

    Empower Introducer Sheath recalled for potential embolism and ischemia risk

    Freudenberg Medical is recalling Empower Introducer Sheath devices (Model 668782-200) due to potential adhesive residue inside the catheter shaft that may cause blood clots and tissue damage. Affected devices were distributed in the US and Netherlands.

    Product
    Empower Introducer Sheath with Hydrophilic Coating 21F x 56cm Model: 668782-200 (OUS)
    Category
    Medical Device
    Distribution
    2 states