FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass II · Medical device · Recalled July 1, 2026

Multi-Snare Set recall — PFM MEDICAL INC.

Hazard: 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.

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
Z-2526-2026
Brand
PFM MEDICAL
Classification
Class II
Units affected
32
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

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

Affected products

Companies & origin

Recalling firm location
Carlsbad, CA, United States
Firm address
1916 Palomar Oaks Way, N/A, 92008-5523

Identifying details (verbatim from the notice)

Product codes / lots
REF/UDI-DI/Lot(Expiration): 147305/04042301061829/1049868(10/14/2028); 147310/04042301033567/1049960(10/20/28)
Distribution
US Nationwide distribution in the states of NY, MD.
Firm notified the public via
N/A
FDA event ID
98942
Recall initiated
April 21, 2026
FDA classified
June 23, 2026
FDA report date
July 1, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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