Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16702 |
| Brand Name: | GE Single Width Airway Module E-miniC and Extension Modules N-FC, N-FCREC |
| Model: | Module E-miniC and Extension Modules N-FC, N-FCREC |
| Affected: | Potentially affected modules were manufactured from February 10, 2012 through October 8, 2012. |
| Software version: | |
| Recalling Organisation: | GE Healthcare Limited Level 7, Vero Centre 48 Shortland St Auckland 1010 |
| Contact Information: | 0800 659 465 |
| Manufacturer: | GE Healthcare Finland Oy |
| Issue: | Failure of the CO2 detector in Single-width Airway and Extension modules may cause a slow continuous decrease of measured Et-/FiCO2 values. Incorrect Et CO2/Fi CO2 value may impair clinical decision making for both mechanically and spontaneously ventilated patients because of incorrect low CO2 values. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 16/5/2014 |
