EQUINOXE SHOULDER COMPONENTS
Report
- Report Number
- 1038671-2023-01114
- Event Type
- Injury
- Date Received
- May 24, 2023
- Date of Event
- April 3, 2023
- Report Date
- September 2, 2025
- Manufacturer
- EXACTECH, INC.
- Product Code
- KWT
- PMA / PMN Number
- UNK
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
D10. CONCOMITANTS: HUMERAL STEM OR STEMLESS 3000111. REVERSE HUMERAL TRAY 3201000. REVERSE GLENOSPHERE 3203236. REVERSE GLENOSPHERE BASEPLATE 3203504.
THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL AND/OR CORRECTED INFORMATION. THE FOLLOWING SECTIONS WERE UPDATED/CORRECTED: D1, D4, G4, H6. MDR SECTION CODES UPDATED/CORRECTED: A, B, C, D, F, G. PMA 510K CANNOT BE DETERMINED; DEVICE IS UNKNOWN. CATALOG NUMBER, UDI NUMBER, SERIAL NUMBER, EXPIRATION AND MANUFACTURED DATES UNKNOWN. THE REASON FOR THE INTRAOPERATIVE BONE FRACTURE REPORTED CANNOT BE CONCLUSIVELY DETERMINED BUT MAY BE RELATED TO A PATIENT CONDITION OR HIGH FORCES DURING BROACHING, REAMING, EXPOSURE, OR RETRACTION. HOWEVER, THIS CANNOT BE CONFIRMED BASED ON THE INFORMATION PROVIDED. IF ANY FURTHER INFORMATION IS OBTAINED THAT WOULD CHANGE OR ALTER ANY INFORMATION PROVIDED, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY.
IT WAS REPORTED VIA CLINICAL STUDY THAT THE 82 YO FEMALE PATIENT EXPERIENCED A SCAPULAR FRACTURE INTRA-OPERATIVELY. THE CORACOID FRACTURE OCCURRED DURING RETRACTOR PLACEMENT AND HAD NOT HAD GPS YET. NO ACTION WAS TAKEN. THE OUTCOME WAS LAST KNOWN AS CONTINUING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 761080 | EQUINOXE SHOULDER COMPONENTS | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED | KWT | EXACTECH, INC. | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 82 YR | Female | Other| R | SEE H10. |