TORNIER PERFORM REVERSED STANDARD GLENOSPHERE DIA 36MM
Report
- Report Number
- 0001649390-2024-00707
- Event Type
- Injury
- Date Received
- December 12, 2024
- Date of Event
- September 13, 2024
- Report Date
- December 12, 2024
- Manufacturer
- TORNIER INC
- Product Code
- PHX
- UDI-DI
- 00846832090334
- PMA / PMN Number
- K161742
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UT, US
- Reporter Occupation
- 501
Narratives
BASED ON THE AVAILABLE INFORMATION THE DEVICE WILL NOT BE RETURNED THEREFORE AN EVALUATION OF THE DEVICE CANNOT BE PERFORMED. A REVIEW OF THE DEVICE HISTORY IS NOT POSSIBLE BECAUSE THE LOT NUMBER WAS NOT COMMUNICATED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, IT WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.
AS REPORTED: "SUBJECT: (B)(6) PHS STUDY: SCAPULAR FRACTURE. PT WAS DOING PLATES AND STRENGTH TRAINING WITH SUDDEN ONSET OF SEVERE LEFT SHOULDER PAIN GOING FROM SORE TO UNABLE TO RAISE LEFT ARM. PATIENT WAS DIAGNOSED WITH AN ACROMIAL FRACTURE (B)(6) 2024 AND RETURNED TO CLINIC (B)(6) 2024 WITH SHOULDER RECOVERING. ACTIONS TAKEN: REHABILITATION (BONE STIMULATOR) & TREATMENT/MEDICATION (SLING AT ALL TIMES, 3-4 WEEKS, DICLOFENAC AND TYLENOL FOR MILD TO MODERATE PAIN). AE UPDATE 14 NOV 2024: DESCRIPTION OF UPDATE: PATIENT HAS RECOVERED WELL AND CLINIC TEAM HAS ADVISED SHE CONTINUES TO TRANSITION INTO ALL ACTIVITIES AS TOLERATED WHILE USING BONE STIMULATOR FOR ANOTHER 6 WEEKS."
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2154220 | TORNIER PERFORM REVERSED STANDARD GLENOSPHERE DIA 36MM | SHOULDER PROSTHESIS, REVERSE CONFIGURATION | PHX | TORNIER INC | UNKNOWN | 00846832090334 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 81 YR | Female | Required Intervention |