FDASeptember 7, 2023device

Fogarty Thru-Lumen Embolectomy Catheter, REF: 12TLW805F35

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

The hazard

Inadvertent release of embolectomy catheters that may experience slower than normal balloon deflation (greater-than 15 seconds).

What to do

FDA enforcement status: Ongoing

Brands named

edwards lifesciencesedwards

UPCs

00690103043532

Recall history

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

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Fogarty Thru-Lumen Embolectomy Catheter, REF: 12TLW805F35 — Recall Details · AllClear