Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21239 |
| Brand Name: | The Zimmer iASSIST Knee System |
| Model: | |
| Affected: | iASSIST Validation Tool, Lot numbers, 130542A1, 140146, 140147, 140407A, 140407B, 140860, 141035, 150120, B150120 |
| Software version: | |
| Recalling Organisation: | Zimmer Biomet New Zealand Company 210 Khyber Pass Road Grafton Auckland |
| Contact Information: | 09 925 5200 |
| Manufacturer: | Zimmer CAS |
| Issue: | There has been an increase in the number of complaints regarding bent or broken Drive Pins of the Validation Tool manufactured with drawing Revision M to P |
| Recall action type: | Alert |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 21/3/2017 |
