Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23088 |
| Brand Name: | DF_Orthopaedic prosthesis implantation instrument, 13180 |
| Model: | |
| Affected: | CORAIL AMT NECK SEG 125D STD All Lots, CORAIL AMT NECK SEG 125D KLA All Lots, CORAIL AMT NECK SEG 135D STD All Lots, CORAIL AMT NECK SEG 135D KHO All Lots, CORAIL AMT NECK SEG 135D SHORT All Lots |
| Software version: | |
| Recalling Organisation: | Johnson & Johnson (NZ) Limited 13a Gabador Place Mt Wellington AUCKLAND 1060 |
| Contact Information: | 0800 922 638 |
| Manufacturer: | DePuy France SA |
| Issue: | The manufacturer has identified the potential for debris/material to be found behind the O-Rings for some CORAIL Neck Trials. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/6/2018 |
