Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20041 |
| Brand Name: | GE Medical CT Lightspeed Family |
| Model: | |
| Affected: | |
| 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 LLC |
| Brand Name: | GE Medical Nuclear Medicine System, Gamma Camera, Stationary |
| Model: | |
| Affected: | |
| 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 Functional Imaging Haifa |
| Issue: | GE has updated the Service Manuals for the LightSpeed CT and Discovery NM to update an incorrect torque value. We are asking our customers to ensure that the organization that services their equipment uses the latest version of the Service Manual to maintain the safe and proper performance of the medical device. Customers can continue to use the devices. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 20/4/2016 |
