Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 13582 |
| Brand Name: | Zimmer Durom Acetabular Cup |
| Model: | All |
| Affected: | All |
| Software version: | |
| Recalling Organisation: | Zimmer Biomet New Zealand Company 210 Khyber Pass Road Grafton Auckland |
| Contact Information: | 09 925 5200 |
| Manufacturer: | Zimmer GmbH |
| Issue: | The device has a cumulative revision rate of 9.6% at 7 years in resurfacing applications and 6.8% at 5 years for Total Conventional Hip Replacement as reported in the 2011 NJRR report. (Note - this product was withdrawn from New Zealand market from 30 June 2011.) |
| Recall action type: | Alert |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Public Recall |
| Date Commenced: | 12/10/2012 |
