FDADecember 2, 2024device

X-Flow prostatectomy catheter, Device Reference Numbers AB6022, AB6024, AB6118, AB6120, AB6122, AB6124, AB6220, AB6222, AB6224, AB6318, AB6320, AB6322, AB6324, AB6418, AB6420, AB6422, AB6424, AB6522, AB6524, AB6A18, AB6A20, AB6A22, AB6A24, AB6C18, AB6C20, AB6C22, and AB6C24.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

A possible sterility issue was detected in Coloplast's facility on some Coloplast products.

What to do

FDA enforcement status: Ongoing

Brands named

coloplast manufacturingcoloplast

UPCs

360004014337736000401435063600040143636360004014372836000401438103600040143902360004014404636000401440913600040144145360004014419036000401443293600040144459

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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X-Flow prostatectomy catheter, Device Reference Numbers AB6022, AB6024, AB6118, AB6120, AB6122, AB6124, AB6220, AB6222, AB6224, AB6318, AB6320, AB6322, AB6324, AB6418, AB6420, AB6422, AB6424, AB6522, AB6524, AB6A18, AB6A20, AB6A22, AB6A24, AB6C18, AB6C20, AB6C22, and AB6C24. — Recall Details · AllClear