Arrow-clark Vectorflow Antegrade And Retrograde Chronic
Summary Arrow International LLC is recalling Arrow-Clark VectorFlow Antegrade and Retrograde Chronic products distributed to hospitals, pharmacies, and laboratories in New Zealand. The products must be returned to the supplier. This is a Class I recall, which is the most serious classification.
- Recalling firm
- Teleflex Medical New Zealand
- Product
- Arrow-Clark VectorFlow Antegrade and Retrograde Chronic. [Device]. Model: Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter and Arrow-Clark VectorFlow Retrograde Chronic Hemodialysis Catheter. Affected: Multiple Product codes
- Reason
- Use of a sheath introducer that does not split as intended during removal may result in immediate procedural complications, such, as resistance during withdrawal, prolonged procedure time, localised pain, minor bleeding, haematoma, or superficial tissue, injury. Application of excessive force during removal may lead to vessel wall injury or significant bleeding requiring medical or, surgical intervention.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-04-22
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/5407ef2d-174c-410a-add6-00ecd8414bfb