Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22011 |
| Brand Name: | Coated Implant_Delta Extend |
| Model: | |
| Affected: | Modular Centered Epiphysis Size 1 HA, Modular Eccentric Epiphysis Size 1 Left HA, Modular Eccentric Epiphysis Size 1 Right HA, Modular Centered Epiphysis Size 2 HA, Modular Eccentric Epiphysis Size 2 Left HA, Modular Eccentric Epiphysis Size 2 Right HA |
| Software version: | |
| Recalling Organisation: | Johnson & Johnson (NZ) Limited 13a Gabador Place Mt Wellington AUCKLAND 1060 |
| Contact Information: | 0800 922 638 |
| Manufacturer: | DePuy France SA |
| Issue: | The manufacturer has determined that lots produced in a specific machine were manufactured in a manner in which the post's diameter is out-of-specification. Further investigation determined that the issue is related to the circularity of the cylinder. The circularity issue may cause the epiphysis to interfere with the stem and the two implants (epiphysis and stem) cannot be assembled. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 21/9/2017 |
