Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22771 |
| Brand Name: | Epicutaneo-cave catheter Neocath in peel pack |
| Model: | All DPX-NT, DPX Bravo, DPX Duo, DPX-MD, Prodigy, Prodigy Advance Systems running enCORE software from version 9.0 to version 10.0. |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Thermo Fisher Scientific New Zealand Ltd 244 Bush Road Albany AUCKLAND |
| Contact Information: | 0800 636 327 |
| Manufacturer: | Vygon SA |
| Issue: | The manufacturer has become aware of a potential issue with : DPX-NT, DPX Bravo, DPX Duo, DPX-MD, Prodigy, Prodigy Advance Systems running enCORE software from version 9.0 to version 10.0, wherein reports may be sent to the PACS under the wrong patient per the DICOM/PACS header. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/4/2018 |
