Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 13837 |
| Brand Name: | Zimmer Ardis Interbody Inserter |
| Model: | Part Number 3256-01 |
| Affected: | All |
| Software version: | |
| Recalling Organisation: | Zimmer Biomet New Zealand Company 210 Khyber Pass Road Grafton Auckland |
| Contact Information: | 09 925 5200 |
| Manufacturer: | Zimmer Spine Inc |
| Issue: | Zimmer has revised the surgical technique guidance to minimise the risk for off-axis loading on the implant during insertion. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 27/11/2012 |
