DONJOY
Received Dec 27, 2024 · Event occurred Dec 4, 2024
Report 9616086-2024-00136 · MDR key 21031121
Device
Generic name
X-rom Post-op Knee Brace
Manufacturer
Djo LlcCatalog number
11-2181-9
Lot number
TJ31726240822
Product problems
- Mechanical Problem
- Unintended System Motion
- No Apparent Adverse Event
- Mechanical Problem
- Unintended System Motion
- No Apparent Adverse Event
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
- No Clinical Signs, Symptoms or Conditions
Narrative
Additional Manufacturer Narrative
IT WAS REPORTED THAT "THE RED BOTTOM FLEXION/EXTENSION STOP WAS FAILING, THE BRACE CONTINUED TO UNLOCK WHILE PATIENT WAS AMBULATING IN THE POSTOP PERIOD. THE PATIENT NOTICED THE ISSUE THE FIRST WEEK OF USAGE. NO INJURIES AND THE PRODUCT HAS BEEN USED FOR 4 WEEKS". THE BRACE HAS NOT BEEN RETURNED FOR EVALUATION. THE ROOT CAUSE OF THE COMPLAINT IS DAMAGED COMPONENT BASED ON OTHER DEVICES THAT HAVE BEEN EVALUATED. THE DEVICES LOCK BUTTON FAILED DURING MANUFACTURING TESTING CONFIRMED TO BE THE SAME MALFUNCTION FOUND IN REPORT NUMBER: 9616086-2023-00007. ADDITIONAL REPORTING ON THIS EVENT WILL BE PROVIDED AS A SUPPLEMENTAL REPORT TO THIS DOCUMENT IF IT BECOMES AVAILABLE.
Description of Event or Problem
IT WAS REPORTED THAT "THE RED BOTTOM FLEXION/EXTENSION STOP WAS FAILING, THE BRACE CONTINUED TO UNLOCK WHILE PATIENT WAS AMBULATING IN THE POSTOP PERIOD. THE PATIENT NOTICED THE ISSUE THE FIRST WEEK OF USAGE. NO INJURIES AND THE PRODUCT HAS BEEN USED FOR 4 WEEKS".