Arrow recalls Percutaneous Thrombolytic Device kits with PTD tip separation risk. Affected units include specific lot numbers and components. Stop using immediately if you own these kits.
The firm received reports indicating PTD tip separation during use.
Arrow is recalling certain Percutaneous Thrombolytic Device kits due to reports of PTD tip separation during use. This could lead to device failure during medical procedures. Affected kits have specific lot numbers and component codes listed in the recall.
The recall reports that the PTD (Percutaneous Thrombolytic Device) tip can separate during use, potentially causing device failure. This could lead to complications during dialysis treatments if the device malfunctions.
Healthcare professionals using the Arrow-Trerotola Percutaneous Thrombolytic Device kits for dialysis treatments are most at risk. Patients receiving these treatments may also be affected if their devices are recalled.
Check for the product name 'Arrow-Trerotola Over-The-Wire PTD Kit' with specific lot numbers listed in the recall. Components include PT-65709-C, PT-03009, and PT-65709-HFS with the listed lot numbers.
Look for the lot number on the device or component packaging to determine if it's affected.
If you have the affected lot numbers, stop using the device immediately to prevent potential failure during medical procedures.
The recall reports that the PTD tip can separate during use, potentially causing device failure during dialysis treatments.
Affected lot numbers include 13F20A0323, 13F20B0139, 13F20C0594, 13F20F0083, 13F20F0230, 13F20F0577, 13F20H0756, 13F20K0849, 13F20L0283, 13F20M0182, 13F21A0498, 13F21B0158, 13F21C0747, and 13F21E0555.
The recall does not specify a return process, but you should stop using the device immediately if it's affected.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0624-2022 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0624-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
