FDAFDA · Food and drugs·Recall number Z-2526-2026
Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310
Published July 1, 2026 · Recall initiated: April 21, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the 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.
What to do
Voluntary: Firm initiated
Recall details
- Manufacturer
- PFM MEDICAL INC.
- Distributor
- US Nationwide distribution in the states of NY, MD.
- Lot
- REF/UDI-DI/Lot(Expiration): 147305/04042301061829/1049868(10/14/2028); 147310/04042301033567/1049960(10/20/28)
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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