Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28170 |
| Brand Name: | DuoDERM Extra Thin |
| Model: | |
| Affected: | Batch number - 9H02226, 9H04865, 9L02456, 9L01731, 9L04890, 9K02656, 9H01234, 9M01779, 9H00183, |
| Software version: | |
| Recalling Organisation: | Convatec (New Zealand) Ltd WHK Gosling Chapman Level 6, 51-53 Shortland Street Auckland |
| Contact Information: | 0800 441 763 |
| Manufacturer: | Convatec Ltd |
| Brand Name: | DuoDERM CGF |
| Model: | |
| Affected: | Batch number - 9B02984Y, 0A03460 |
| Software version: | |
| Recalling Organisation: | Convatec (New Zealand) Ltd WHK Gosling Chapman Level 6, 51-53 Shortland Street Auckland |
| Contact Information: | 0800 441 763 |
| Manufacturer: | Convatec Ltd |
| Issue: | The manufacturer has received reports for DuoDerm CGF, where the packaging layers were not sealed together completely, leaving a partial or open seal after manufacturing which may lead to lack of sterility |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 10/8/2021 |
