Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20751 |
| Brand Name: | Abbott Spine France - Instruments |
| Model: | |
| Affected: | Wallis Prosterior Dynamic Stabilization System instruments and containers, all lots |
| Software version: | |
| Recalling Organisation: | Zimmer Biomet New Zealand Company 210 Khyber Pass Road Grafton Auckland |
| Contact Information: | 09 925 5200 |
| Manufacturer: | Zimmer Spine |
| Issue: | The manufacturer has updated cleaning and disinfection instruction for the Wallis Posterior Dynamic Stabilization System (IFU,002WNAN0000T rev 2) |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 20/10/2016 |
