FDA Adverse Event Injury Summary report: N

BMT SPLINED KNEE STM V2 20X80

MDR report key: 21448185 · Received February 24, 2025

Report

Report Number
0001825034-2025-00444
Event Type
Injury
Date Received
February 24, 2025
Report Date
July 21, 2025
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JWH
UDI-DI
00880304528895
PMA / PMN Number
K121149
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

CMP-0977539 D10-MEDICAL PRODUCT VG 360 UNIV PST FM AUG 70X5, ITEM# 185346, LOT# 138350. VNGD TI FEM SSK 70MM LT, ITEM# CP113127, LOT# 795410. BMT SPLINED KNEE STM V2 20X120, ITEM# 148323, LOT# 855010. BIOMET OFFSET TIBIAL TRAY 71MM, ITEM# 141483, LOT# 866560. OFFSET TIB TRAY NEUT ADAPTOR, ITEM# 141489, LOT# 146410. UNKNOWN ARTICULAR SURFACE. H3- CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED.

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. UPDATED: A4, B4, B5, B7, D2, E1, E2, E3, E4, G1, G2, G3, G6, H1, H2, AND H11. CORRECTION: D6A.

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. UPDATED: B4, B5, B7, D2, G1, G3, G6, H1, H2, H6, AND H11.

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. UPDATED: B4, B5, B7, D2, G1, G3, G6, H1, H2, H3, H6, AND H11. NO PRODUCT WAS RETURNED, OR PICTURES PROVIDED; THEREFORE, VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. MEDICAL RECORDS/RADIOGRAPHS WERE PROVIDED AND REVIEWED BY A HEALTH CARE PROFESSIONAL. REVIEW OF THE AVAILABLE RECORDS IDENTIFIED THE FOLLOWING: ¿ MOTION HAS IMPROVED "SHE FEELS LIKE SHE COULD HAVE PLACED IN HER KNEE AT ALL TIMES. SHE IS ON PT. SHE TRIED COMPRESSION SLEEVES, BUT NOTHING SEEMS TO BE HELPING. SHE TRIED MELOXICAM WHICH DID NOT HELP," NOT CALLING OUT ADDITIONAL SYMPTOMS/OUTCOMES AS ALLEGATION IS UNCLEAR FROM STATEMENT DICTATED. ¿ INCISION C/D/I-NO SIGNS OF INFECTION, MILD SWELLING WITHIN NORMAL LIMITS, ROM 0-125DEG. ¿ PATELLA TRACKS SMOOTHLY, EXCELLENT OVERALL ALIGNMENT, KNEE IS STABLE. ¿ OVERALL PATIENT IS DOING WELL. THE FEELING OF A VICE AROUND HER KNEE IS VERY DIFFICULT TO FIGURE OUT. IT IS HARD TO TELL IF INFLAMMATION OR JUST SCAR TISSUE PRESENT. A CORTISONE SHOT WAS OFFERED, AND CELEBREX HAS BEEN PRESCRIBED. RADIOGRAPH REPORT, THREE VIEWS OF L KNEE. ¿ EXCELLENT OVERALL ALIGNMENT. ¿ NO EVIDENCE OF POST-OPERATIVE COMPLICATIONS. ¿ NO EVIDENCE OF EARLY SUBSIDENCE OR LOOSENING. ¿ NO EVIDENCE OF FRACTURE OR IMPLANT COMPLICATION. ¿ NORMAL APPEARING POST-OP TOTAL KNEE IMAGES. DEVICE HISTORY RECORD (DHR) WAS REVIEWED FOR DEVIATIONS AND/ OR ANOMALIES WITH NO DEVIATIONS / ANOMALIES IDENTIFIED. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED. THIS COMPLAINT IS CONFIRMED THROUGH THE MEDICAL RECORDS. IF ANY FURTHER INFORMATION IS RECEIVED WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL MEDWATCH WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. H6: COMPONENT CODE: PROPOSED COMPONENT (ANNEX G) CODE IS: - MECHANICAL (G04) ¿ STEM.

Description of Event or Problem · 0

IT WAS REPORTED THAT A PATIENT IS EXPERIENCING PAIN AND AMBULATION DIFFICULTIES APPROXIMATELY TWO YEARS AND TWO AND A HALF MONTHS POST IMPLANTATION. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE INFORMATION IS AVAILABLE AT THIS TIME.

Description of Event or Problem · 0

NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

Description of Event or Problem · 0

IT WAS REPORTED THAT A PATIENT IS EXPERIENCING PAIN AND AMBULATION DIFFICULTIES APPROXIMATELY TWO YEARS AND TWO AND A HALF MONTHS POST IMPLANTATION. AT FOLLOW-UP VISIT A CORTISONE SHOT WAS OFFERED AND CELEBREX HAS BEEN PRESCRIBED. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE INFORMATION IS AVAILABLE.

Description of Event or Problem · 0

NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
404064 BMT SPLINED KNEE STM V2 20X80 PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. 102900 00880304528895

Patients

Seq Age Sex Outcome Treatment
1 NA Female Other SEE H11