Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 18279 |
| Brand Name: | Covidien Trellis Peripheral Infusion System |
| Model: | All Trellis 6 and Trellis 8 products |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Covidien NZ Ltd Level 3, Building 5, Central Park Corporate Centre 666 Great South Road Penrose AUCKLAND 1051 |
| Contact Information: | 0508 489 264 |
| Manufacturer: | Covidien LLC |
| Issue: | The manufacturer has advised there is the potential for a sterility breach of the outer packaging or pouch material of all lots manufactured. This breach of the outer pouch does not directly affect the sterility of the device components within the inner pouch, but may compromise the outer surface sterility of the inner pouch and so the sterility of the contents when the pouch is opened could potentially contaminate the sterile field and sterile personnel. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 26/3/2015 |
