Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14384 |
| Brand Name: | GE Dash 3000/4000/5000 Patient Monitor |
| Model: | Product codes include SHQ and SD0 |
| Affected: | Units manufactured between Oct-2010 and Sep-2012 |
| Software version: | |
| Recalling Organisation: | GE Healthcare Limited Level 7, Vero Centre 48 Shortland St Auckland 1010 |
| Contact Information: | 0800 659 465 |
| Manufacturer: | GE Medical Systems Information Technologies Inc |
| Brand Name: | GE Patient Data Module (PDM) |
| Model: | Product codes include SA3 |
| Affected: | Units manufactured between Oct-2010 and Sep-2012 |
| Software version: | |
| Recalling Organisation: | GE Healthcare Limited Level 7, Vero Centre 48 Shortland St Auckland 1010 |
| Contact Information: | 0800 659 465 |
| Manufacturer: | GE Medical Systems Information Technologies Inc |
| Brand Name: | GE TRAM Patient Monitor |
| Model: | Models 451, 451N, 451M, 851, 851N, 851M, 451N5, 851N5 |
| Affected: | Units manufactured between Dec-2010 and Sep-2012 |
| Software version: | |
| Recalling Organisation: | GE Healthcare Limited Level 7, Vero Centre 48 Shortland St Auckland 1010 |
| Contact Information: | 0800 659 465 |
| Manufacturer: | GE Medical Systems Information Technologies Inc |
| Issue: | ECG and Respiration signal noise caused by DASH and PDM ECG cable connector movement may result in reduced ECG, Respiration and arrhythmia detection performance. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 21/3/2013 |
