Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25245 |
| Brand Name: | Friendly Femoral Stem |
| Model: | |
| Affected: | All lot numbers manufactured starting from 03/08/2019 |
| Software version: | |
| Recalling Organisation: | Enovis Surgical NZ Ltd 46 Hillside Road Wairau Valley AUCKLAND 0627 |
| Contact Information: | 09 3606010 |
| Manufacturer: | Limacorporate SpA |
| Brand Name: | H Max C Femoral Stem |
| Model: | |
| Affected: | All lot numbers manufactured starting from 03/08/2019 |
| Software version: | |
| Recalling Organisation: | Enovis Surgical NZ Ltd 46 Hillside Road Wairau Valley AUCKLAND 0627 |
| Contact Information: | 09 3606010 |
| Manufacturer: | Limacorporate SpA |
| Issue: | The manufacturer has identified that instruction for use related to LimaCorporate monolithic cementless and cemented femoral stems were reviewed in order to be aligned with the requirements posed by the ISO standards aimed at promoting global harmonization on mechanical testing matter related to orthopedic implants. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 18/10/2019 |
