FDA Adverse Event Injury Summary report: N

10MM RS AVL TIB BRNG

MDR report key: 24923962 · Received April 20, 2026

Report

Report Number
0001825034-2026-00964
Event Type
Injury
Date Received
April 20, 2026
Report Date
April 20, 2026
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JWH
PMA / PMN Number
UNKNOWN
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

(B)(4). D10: PN: CP111207, LN: 885120, CUSTOM AVL TIBIAL BUSHING SET. PN: CP561286, LN: 883640, 9MM SHORT CPS ANCHOR PLUG. PN: CP115759, LN: 077630, 9X25MM 400LB SHRT CPS SPDL. PN: CP114019, LN: 885170, 10MM RS AVL TIB BRNG. PN: CP115761, LN: 077530, CUST 10MM RS AVL YOKE. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED.

Description of Event or Problem · 0

IT WAS REPORTED PATIENT IS BEING CONSIDERED FOR A REVISION DUE TO DECREASED RANGE OF MOTION. NO REVISION HAS BEEN REPORTED TO DATE. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
983357 10MM RS AVL TIB BRNG PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. 885170

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Other SEE H11.