Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36916 |
| Brand Name: | CS - EOPA 3D Arterial Cannula |
| Model: | 78222 and 78322 |
| Affected: | 0232612916, 0233245850, 0233245860, 0232862787 |
| Software version: | |
| Recalling Organisation: | Medtronic New Zealand Limited Unit 16 Mezzanine Level 5 Gloucester Park Road Onehunga AUCKLAND |
| Contact Information: | 0800 377 807 |
| Manufacturer: | Medtronic Inc |
| Brand Name: | CS - EOPA Elongated One-Piece Arterial Cannulae |
| Model: | 77422, 77522, 77622, 77722 |
| Affected: | 0233009922, 0233116991, 0232798265, 0232902803, 0232601516, 0232601586, 0232601591, 0233009922, 0233528727, 0232990983,0232709428, 0232990983, 0232862794,0232862798, 0233286414, 0232745092, 0232903291, 0232601549, 0232602178, 0232744945 |
| Software version: | |
| Recalling Organisation: | Medtronic New Zealand Limited Unit 16 Mezzanine Level 5 Gloucester Park Road Onehunga AUCKLAND |
| Contact Information: | 0800 377 807 |
| Manufacturer: | Medtronic Inc |
| Issue: | 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. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 22/6/2026 |
