FDAJanuary 11, 2022device

Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (A...

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

10801902121315

Recall history

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

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