FDA Adverse Event Injury Summary report: N

TORNIER PERFORM ANATOMIC GLENOID CORTILOC PEGGED S40

MDR report key: 24817351 · Received April 8, 2026

Report

Report Number
3000931034-2026-00334
Event Type
Injury
Date Received
April 8, 2026
Date of Event
February 19, 2026
Report Date
April 8, 2026
Manufacturer
TORNIER S.A.S.
Product Code
KWS
UDI-DI
03700434019667
PMA / PMN Number
K111902
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

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.

Description of Event or Problem · 0

SUBJECT: (B)(6). PHS STUDY. (B)(6) 2026. TRAUMATIC FALL. PARTICIPANT SUSTAINED A FALL ON SHOULDER WHILE WALKING DOG. X-RAY AND MUSCULOSKELETAL ULTRASOUND FINDINGS DEMONSTRATE INTACT SOFT TISSUE AND NO RELATIVE CHANGES TO IMPLANT. THEY REPORT INCREASED PAIN SINCE FALL. (B)(6) 2026. PARTICIPANT WAS DRYING HAIR AND FELT "SNAP" IN SHOULDER WITH EXCRUCIATING PAIN. PHYSICAL EXAM NEGATIVE FOR SOFT TISSUE DAMAGE. WILL REPEAT MSK ULTRASOUND ON 1MAR2026 IF PAIN PERSISTS. UPDATE #2 ((B)(6) 2026) REPEAT MUSCULOSKELETAL ULTRASOUND NEGATIVE FOR SOFT TISSUE DAMAGE OR DEVICE ISSUES. AN UNRECOGNIZABLE MASS IS PRESENT BETWEEN LESSER AND GREATER TUBEROSITIES. UPDATE 3 ((B)(6) 2026): CT FINDINGS AND SURGERY. NOT RELATED TO DEVICE/POSSIBLY RELATED TO PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
472308 TORNIER PERFORM ANATOMIC GLENOID CORTILOC PEGGED S40 PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED KWS TORNIER S.A.S. UNKNOWN 03700434019667

Patients

Seq Age Sex Outcome Treatment
1