Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28541 |
| Brand Name: | Nuvasive PRECICE System |
| Model: | |
| Affected: | Multiple Item numbers |
| 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: | Additional biological assessments (carcinogenicity, chronic toxicity, developmental toxicity, and reproductive toxicity) have now been completed and the IFU for Precice IMLL System devices has been updated again to include: Clarity on indication for use in adults; Warning that no more than two (2) devices should be implanted at one time and a patient must be greater than 50 lbs.; and Addition of Potential Adverse Events section. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 3/11/2021 |
