Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36922 |
| Brand Name: | Horus TMC |
| Model: | HORUS TMC cup |
| Affected: | LOT numbers: 2010965, 2016014, 2017024, 2022633, 2021733 |
| Software version: | |
| Recalling Organisation: | Evolutis New Zealand Limited Unit 19, 150 Cavendish Road Casebrook Christchurch 8051 |
| Contact Information: | |
| Manufacturer: | Evolutis |
| Issue: | The device size is engraved on the back of the insert. A deviation has been observed in the depth of this engraving, which poses a potential risk of the thickness being less than the approved thickness. The potential consequence is premature wear of the insert. All new batches manufactured since May 2026 comply with the requirements (no size engraving). Affected product that has not been implanted has been destroyed and replaced with new the new batch references so you will not receive any affected batches moving forward. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 29/6/2026 |
