MEDLINE
Received Jul 31, 2026 · Event occurred Feb 24, 2025
Report 1417592-2026-12255 · MDR key 50105082
Device
Product problems
- Fracture
Patient
Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
It was reported that they had a broken tie rod for the left arm that made it so it could not move. Now the right side had the exact same thing happen.
Additional Manufacturer Narrative
It was reported that they had a broken tie rod for the left arm that made it so it could not move. Now the right side had the exact same thing happen. There were no reports of death, serious injury, medical intervention, or follow up care. It has been determined that the reported event could cause or contribute to serious injury if it were to occur again. In an abundance of caution, this is a reportable event. If additional information becomes available this report will be reopened and reevaluated. This Medical Device Report (MDR) is being submitted as part of retrospective review activities, which include review of historical data in accordance with regulations at 21 CFR Part 803. The information included in this MDR reflects the information reasonably known to the manufacturer at the time of this retrospective review and submission.