Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 18294 |
| Brand Name: | Transonic Hemodialysis Monitor |
| Model: | Catalogue Number: HD03 |
| Affected: | Lot Numbers: A81225, A91394 & B21812 |
| Software version: | |
| Recalling Organisation: | TekMed NZ Pty Ltd Hilary Square Orewa Orewa 0946 |
| Contact Information: | 0800 456 217 |
| Manufacturer: | Transonic Systems Inc |
| Issue: | This recall is being initiated because of customer complaints indicating the inability to obtain measurements due to the device sometimes seeing no flow or irrelevant flow condition when used with patients during dialysis procedures. No reports of injuries have been reported nor are expected due to the nature of this issue. The problem is readily identified to the user by a zero or a very low flow value displayed on HD03 and/or no measurements produced in other modes (recirculation; access flow; or cardiac output). |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/3/2015 |
