FDAJanuary 11, 2022device

Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic di...

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

The hazard

The firm received reports indicating PTD tip separation during use.

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

UPCs

00801902013156108019020131531080190219407420801902194071

Recall history

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

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Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic di... — Recall Details · AllClear