Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14572 |
| Brand Name: | GE LOGIQ S8 and LOQIQ S7 Ultrasound |
| Model: | |
| Affected: | with software revisions R.1.1.1 , R1.5.1 and R1.0.1, R1.0.2 and R1.0.3 |
| Software version: | |
| Recalling Organisation: | GE Healthcare Limited Level 7, Vero Centre 48 Shortland St Auckland 1010 |
| Contact Information: | 0800 659 465 |
| Manufacturer: | GE Ultrasound Korea Ltd |
| Issue: | Manufacturer has recently become aware of a potential safety issue due to the S4-10-D Ultrasound Probe used in conjunction with the LOGIQ S8 and LOGIQ S7 Ultrasound systems. It was also discovered that this issue also leads to a specification issue of the acoustic output of this probe There is a potential for a skin burn when the flow model in the cardiac application is activated with the S4-10-D Ultrasound Probe. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/4/2013 |
