FDA Adverse Event Injury Summary report: N

EQUINOXE SHOULDER COMPONENTS

MDR report key: 16998051 · Received May 24, 2023

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

Additional Manufacturer Narrative · 0

D10. CONCOMITANTS: HUMERAL STEM OR STEMLESS 3000111. REVERSE HUMERAL TRAY 3201000. REVERSE GLENOSPHERE 3203236. REVERSE GLENOSPHERE BASEPLATE 3203504.

Additional Manufacturer Narrative · 0

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.

Description of Event or Problem · 0

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.