FDA Adverse Event Injury Summary report: N

UNKNOWN ARTICULAR SURFACE

MDR report key: 24746157 · Received March 31, 2026

Report

Report Number
0001822565-2026-01026
Event Type
Injury
Date Received
March 31, 2026
Date of Event
May 28, 2025
Report Date
March 31, 2026
Manufacturer
ZIMMER BIOMET, INC.
Product Code
MBH
PMA / PMN Number
NI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

(B)(4). D4: ATTEMPTS HAVE BEEN MADE TO GATHER ALL PRODUCT IDENTIFICATION INFORMATION, AND NO FURTHER INFORMATION HAS BEEN PROVIDED. D10: UNKNOWN - UNKNOWN TIBIA - UNKNOWN. UNKNOWN - UNKNOWN FEMORAL - UNKNOWN. UNKNOWN - UNKNOWN FEMORAL STEM - UNKNOWN. UNKNOWN - UNKNOWN TIBIA STEM - UNKNOWN. G2: FOREIGN - EVENT OCCURRED IN CANADA. G2: LITERATURE - GREENBERG, A., BRAUNSTEIN, D., ABUGHADUMA, N.R., GROSS, A., SAFIR, O., KUZYK, P., WOLFSTADT, J., BACKSTEIN, D. (2025). SURVIVORSHIP AND COMPLICATIONS IN REVISION TOTAL KNEE ARTHROPLASTY WITH A CONSTRAINED CONDYLAR KNEE IMPLANT: A MINIMUM 10-YEAR FOLLOW-UP STUDY. THE JOURNAL OF ARTHROPLASTY, VOLUME 40, ISSUE 12, 3240 - 3245. DOI: 10.1016/J.ARTH.2025.05.088. 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.

Description of Event or Problem · 0

IT WAS REPORTED IN A JOURNAL ARTICLE THAT THREE PATIENTS EXPERIENCED MINOR INFECTIONS AND LOCALIZED PAIN WHICH WERE TREATED CONSERVATIVELY WITHOUT FURTHER SURGICAL INTERVENTION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
800513 UNKNOWN ARTICULAR SURFACE PROSTHESIS, KNEE MBH ZIMMER BIOMET, INC. UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention