CASE ALERT: Arrow-Trerotola Over-The-Wire (PTD) Kit
Percutaneous Thrombolytic Device: 7FR Lawsuits
Our team of attorneys is currently investigating claims that the Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR has a risk of the catheter’s tip separating from the basket.

CASE ALERT: Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR Lawsuits
Our team of attorneys is currently investigating claims that the Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR has a risk of the catheter’s tip separating from the basket.
Were you harmed by an Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR? Call ASK LLP today at (877) RING ASK (877-746-4275) for a free case evaluation.
What We Know About Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR
The Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR Catheter is used to remove blood clots in adult patients who have an arterio-venous (AV) fistula or synthetic dialysis graft. According to the Mayo Clinic, patients who have an AV fistula or synthetic dialysis graft are generally undergoing hemodialysis, treating for severe kidney disease.
On November 18, 2021, the FDA issued a Class I recall, warning that Arrow International Inc. is recalling certain lots of the arterial catheter due to risk of the device tip separating from the basket. The recall warns that if the orange inner lumen of the tip separates from the basket, it “may lead to serious adverse events” including:
- Vessel damage
- Need for additional medical procedures
- Death
Indeed, a Class I recall means that “use of these devices may cause serious injury or death.” The recall states that a total of 3,241 devices are subject to this recall, identifying recalled devices by lot number.
On February 24, 2022, FDA MedWatch sent a bulletin reporting that as of December 2021, it has received a total of 35 complaints of tip separation, including 14 reported injuries.
Recoverable Compensation in an Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR Lawsuit
If you or a loved one suffered harm after being treated using an Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR, then you may be eligible to participate in a lawsuit against the device’s manufacturers and sellers. If you hire ASK LLP, we will seek the following damages for you:
- Past and future medical expenses
- Past and future pain and suffering
- Past and future wage loss
- Past and future loss of earning capacity
- Past and future loss of enjoyment of life
- Punitive damages, if justified
CALL TODAY! If you or a loved one were treated using an Arrow-Trerotola Over-The-Wire (PTD) Kit Percutaneous Thrombolytic Device: 7FR, you may be entitled to compensation. Call ASK LLP at (877) RING ASK (877-746-4275) for a free case evaluation.
Why You Should Choose ASK LLP
When you get hurt by a medical device, you may not know what to do. After all, the medical device industry is a large and powerful one. We are here to help. Our experienced legal team has a strong track record of fighting—and winning—against big medical device companies. If you hire us, know that we will fight tirelessly to get you the best possible result.
Have you suffered an Arrow-Trerotola PTD injury
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