Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14560 |
| Brand Name: | Terumo Trima Accel Automated Blood Collections System |
| Model: | 81000 |
| Affected: | 1T05282 |
| Software version: | |
| Recalling Organisation: | The Advisory Group Ltd Level 9 55 Shortland St Auckland 1010 |
| Contact Information: | |
| Manufacturer: | Terumo BCT Inc |
| Issue: | Recall for Product Correction for the addition of a safety enhancement called Air Reduction Mitigation (ARM). This safety enhancement is being implemented to address the potential risk for air embolism should a donor be prematurely connected to the Trimal Accel System. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/5/2013 |
