CHATTANOOGA
Received Nov 7, 2024 · Event occurred Oct 11, 2024
Report 9616086-2024-00098 · MDR key 20627257
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Insufficient Information
- Insufficient Information
Narrative
Additional Manufacturer Narrative
IT WAS REPORTED THAT UNIT ERRORED DURING TREATMENT, THE CLINICIAN WENT TO REMOVE ROPE, BUT IT JERKED BACK INTO THE UNIT PULLING THE DOCTORS ARM AND PATIENTS HEAD. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION, COMPLAINT COULD NOT BE CONFIRMED. THE ROOL CAUSE COULD NOT BE ESTABLISHED. IF MORE INFORMATION BECOMES AVAILABLE ADDITIONAL REPORTING ON THIS EVENT WILL BE PROVIDED AS A SUPPLEMENTAL REPORT TO THIS DOCUMENT.
Description of Event or Problem
IT WAS REPORTED THAT UNIT ERRORED DURING TREATMENT, THE CLINICIAN WENT TO REMOVE ROPE, BUT IT JERKED BACK INTO THE UNIT PULLING THE DOCTORS ARM AND PATIENTS HEAD.