FDA Adverse Event Injury Summary report: N

UNKNOWN TRILOGY CUP

MDR report key: 7069132 · Received November 29, 2017

Report

Report Number
0001822565-2017-08133
Event Type
Injury
Date Received
November 29, 2017
Date of Event
March 23, 2017
Report Date
November 28, 2017
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). UNKNOWN, UNKNOWN TRILOGY LINER, UNKNOWN. REPORT SOURCE, FOREIGN ¿ EVENTS OCCURRED IN THE UNITED KINGDOM, AUSTRALIA, FINLAND, AND DENMARK. REPORT SOURCE, LITERATURE - HUGHES, R. E., BATRA, A., & HALLSTROM, B. R. (2017). ARTHROPLASTY REGISTRIES AROUND THE WORLD: VALUABLE SOURCES OF HIP IMPLANT REVISION RISK DATA. CURRENT REVIEWS IN MUSCULOSKELETAL MEDICINE, 10(2), 240-252. DOI:10.1007/S12178-017-9408-5. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. ROOT CAUSE WAS UNABLE TO BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001822565 - 2017 - 08134. PRODUCT LOCATION UNKNOWN.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT 17,473 PATIENTS WERE REVISED DUE TO UNKNOWN REASONS. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
845853 UNKNOWN TRILOGY CUP PROSTHESIS, HIP JDI ZIMMER BIOMET, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R