Arrow recalls 7FR Percutaneous Thrombolytic Devices (PTD) with risk of inner lumen detachment causing embolization and delayed therapy. Affected units have specific product codes and lot numbers.
7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached from the device basket result in embolization and retrieval with an additional intervention and consequent delay of therapy.
Arrow is recalling certain Percutaneous Thrombolytic Devices (PTDs) because the inner lumen (orange part) can detach from the device basket. This detachment may cause blood clots to travel and require additional medical procedures, delaying treatment.
The inner lumen (orange section) can detach from the device basket during use. This detachment may cause blood clots to travel through the bloodstream, requiring additional medical intervention and delaying critical treatment.
Healthcare professionals using the Arrow-Trerotola PTD kit for dialysis treatments are most at risk. Patients receiving these devices during procedures may experience delayed therapy if the inner lumen detaches.
Check for product codes PT-65709-HFWC and lot numbers listed in the description (e.g., 13F19K0369, 13F20A0323). The device is used in dialysis treatments and sold by Arrow International.
Look for lot numbers on the device packaging or label, such as 13F19K0369 or 13F20A0323.
Reach out to Arrow International for specific guidance on the recall and next steps.
The product code is PT-65709-HFWC.
Detachment can cause blood clots to travel, requiring additional medical procedures and delaying treatment.
Check for product code PT-65709-HFWC and lot numbers like 13F19K0369 or 13F20A0323.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0232-2022 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0232-2022 from Arrow. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
