FDAJanuary 11, 2022device

Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-12709-CA, PT-12709-C, The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native ...

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

2080190215675810801902121254

Recall history

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

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