FDA Adverse Event Injury Summary report: N

UNKNOWN CUP

MDR report key: 8663392 · Received June 3, 2019

Report

Report Number
0001822565-2019-02288
Event Type
Injury
Date Received
June 3, 2019
Report Date
June 3, 2019
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
PMA / PMN Number
NI
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CT, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: ITEM# UNKNOWN UNKNOWN LINER LOT# UNKNOWN, ITEM# UNKNOWN UNKNOWN HEAD LOT# UNKNOWN. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: LINER: 0001822565-2019-02288, HEAD: 0001822565 -2019 -02159 -1. REPORTED EVENT WAS CONFIRMED BY REVIEW OF RADIOGRAPHS. RADIOGRAPHS WERE PROVIDED AND REVIEWED BY A HEALTH CARE PROFESSIONAL. REVIEW OF THE AVAILABLE RECORDS IDENTIFIED THE FOLLOWING: MALPOSITION OF ACETABULAR CUP WITH VERTICAL POSITION, LIKELY PREDISPOSING TO DISLOCATION. THERE WAS SUPERIOR DISLOCATION OF THE FEMORAL HEAD. POSSIBLE FRACTURE ALONG INTERTROCHANTERIC REGION. 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.

Description of Event or Problem · 1

IT WAS REPORTED THAT PATIENT SUFFERED A DISLOCATION AND WAS CONSIDERING REVISION SURGERY. ATTEMPTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION; HOWEVER NONE WAS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
455556 UNKNOWN CUP PROSTHESIS, HIP JDI ZIMMER BIOMET, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Other