Class II
Medical Device Recall: Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310
PFM MEDICAL INC. · April 21, 2026
Reason for Recall
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.
Distribution
US Nationwide distribution in the states of NY, MD.
States Affected
NATIONWIDE
Quantity Affected
32
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2526-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.