Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 19936 |
| Brand Name: | Maquet Cardiosave Hybrid and Rescue IABP |
| Model: | FLOW-i C20 FLOWE-i C30 and FLOW-i C40 |
| Affected: | Part Nos: 66 77 200 ,66 77 300 and 66 77 400 |
| Software version: | |
| Recalling Organisation: | Maquet Australia Pty Ltd (NZ) 12G Andromeda Cres East Tamaki Auckland 2013 |
| Contact Information: | 021 874 882 |
| Manufacturer: | Maquet Critical Care AB |
| Issue: | The alarm TE63/64 is generated during some circumstances when the FLOW -i-Anaesthesia Systems considers that the internal communication does not work as intended. This falsely triggered technical alarm results in that the vaporiser is turned off due to burning issue between the sub systems. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 24/3/2016 |
