Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 27416 |
| Brand Name: | Nuvasive PRECICE System |
| Model: | P10.7-80V275 |
| Affected: | 001082AAA |
| Software version: | |
| Recalling Organisation: | Lifehealthcare Ltd New Zealand Unit E 61 Hugo Johnston Drive Penrose Auckland 1642 |
| Contact Information: | |
| Manufacturer: | Nuvasive Specialized Orthopaedics Inc |
| Issue: | The manufacturer is notifying all Healthcare providers that Instructions for Use (IFU) for Precice IMLL System has been updated to include the following warning: The PRECICE System has not been evaluated for biological safety in patients in relation to reproductive health or in patients under the age of 18 years of age. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 12/3/2021 |
