Cs - Eopa 3d Arterial Cannula
- Recalling firm
- Medtronic New Zealand Limited
- Product
- CS - EOPA 3D Arterial Cannula. [Device]. Model: 78222 and 78322; 77422, 77522, 77622, 77722. Affected: 0232612916, 0233245850, 0233245860, 0232862787; 0233009922, 0233116991, 0232798265, 0232902803, 0232601516, 0232601586, 0232601591, 0233009922, 0233528727, 0232990983,0232709428, 0232990983, 0232862794,0232862798, 0233286414, 0232745092, 0232903291, 0232601549, 0232602178, 0232744945. Also covers: CS - EOPA Elongated One-Piece Arterial Cannulae
- Reason
- The manufacturer received reports of pinhole leaks in the wire-wound body of 22 Fr EOPA 3D® Arterial Cannulae and EOPA™ Elongated One-Piece Arterial Cannulae used during cardiopulmonary bypass procedures. The leaks were identified either prior to use or during active bypass flow.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-06-22
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/cf6aecec-70da-4e86-be79-6c7bbe1bb67e