Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23222 |
| Brand Name: | Cook Europe Embolization Implant Inserter |
| Model: | |
| Affected: | Label and IFU update |
| Software version: | |
| Recalling Organisation: | Obex Medical Ltd Level 3, 109 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | 0800 656 539 |
| Manufacturer: | William Cook Europe ApS |
| Brand Name: | Cook Europe Embolization Coils |
| Model: | |
| Affected: | IFU update |
| Software version: | |
| Recalling Organisation: | Obex Medical Ltd Level 3, 109 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | 0800 656 539 |
| Manufacturer: | William Cook Europe ApS |
| Issue: | The manufacturer will be implementing a new revision of the Instructions for Use (IFU) for the MReye Flipper PDA Closure Detachable Coil and Flipper 35 PDA Closure Detachable Coil Delivery System. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 26/6/2018 |
