Reported Jul 1, 2026 · Ongoing · Updated Sep 16, 2026

Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310

Pfm Medical Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: PFM MEDICAL INC. · 1916 Palomar Oaks Way · Carlsbad, CA · 92008-5523

Is this the product you have?

  • Multi-Snare Set5 mm x 125 cm
  • REF
    • 147305
    • 10 mm x 125 cm
  • REF147310
Lot codes and dates

2 of 2 products · 2 lot codes

Recalled lot codes, grouped by product number
REFUDI-DILot (Expiration)
14730504042301061829
  • 104986810/14/2028
14731004042301033567
  • 104996010/20/28
Amount recalled
32

Where it was sold

Why it was recalled

A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with a patient's vasculature could result in localized inflammation and tissue irritation.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 7:14 PM UTC

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