Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16416 |
| Brand Name: | KCI Prevena Incision Management System |
| Model: | PRE101 |
| Affected: | |
| Software version: | |
| Recalling Organisation: | InterMed Medical Ltd 71 Apollo Drive Albany AUCKLAND 1311 |
| Contact Information: | 0800 333 444 |
| Manufacturer: | KCI USA Inc |
| Issue: | The manufacturer advised that they have become aware that defects (bulging, gaps, etc) are found in some of the connectors on the dressing in the Prevena Incision Management Kit |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 10/4/2014 |
