FDAJanuary 11, 2022device

5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC containing components: PT-03000, PT-65509-S (PT-65509-S2 alternative), PT-01000-D (PT-01000-D2 alternative) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow ...

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

1080190212128510801902194081

Recall history

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

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