FDA Adverse Event Injury Summary report: N

BIOMET MODULAR FINNED STEM 40MM

MDR report key: 8743886 · Received June 28, 2019

Report

Report Number
0001825034-2019-02710
Event Type
Injury
Date Received
June 28, 2019
Report Date
July 25, 2019
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JWH
PMA / PMN Number
K171054
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

(B)(4). UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THE REPORTED DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE EVENT.

Description of Event or Problem · 0

UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THE REPORTED DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE EVENT.

Additional Manufacturer Narrative · 1

(B)(4). CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION AS THE PRODUCTS REMAIN IMPLANTED. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. . FEMORAL ITEM # 184530 LOT # 596630 , TIBIAL TRAY ITEM # 141274 LOT # 127910, PATELLA ITEM # 141357 LOT # 778860. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2019-02708, 0001825034-2019-02709, 0001825034-2019-02711.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT UNDERWENT LEFT TOTAL KNEE ARTHROPLASTY APPROXIMATELY 3.5 YEARS AGO; SUBSEQUENTLY THE PATIENT IS BEING REVISED FOR UNKNOWN REASON AT A FUTURE DATE. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
538413 BIOMET MODULAR FINNED STEM 40MM PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. N/A 479370

Patients

Seq Age Sex Outcome Treatment
1 78 YR Required Intervention