Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 15629 |
| Brand Name: | Welch Allyn Propaq LT/ Propaq 802 Patient Monitor |
| Model: | 802LTAN, 802LTON, 802LTRN |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Medxus Ltd Unit 4 100 Fitgerald Avenue Christchurch 8011 |
| Contact Information: | 03 365 7403 |
| Manufacturer: | Welch Allyn Protocol Inc |
| Issue: | Internal serial testing has identified fault conditions relating to hardware or software failure or electrical noise caused by proximal defibrillation activity that could, in rare instances, potentially interrupt PROPAQ LT device operations. If this were to occur the device would either present an error screen instructing the user to restart the monitor, or could present a blank screen or white screen.Either screen would be accompanied by one or more blimking LED lights, and in either case, the isue would be resolved by restarting (power cycling) the monitor. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 15/11/2013 |
