FDA Adverse Event Injury Summary report: N

UNKNOWN LINER

MDR report key: 6794210 · Received August 15, 2017

Report

Report Number
0001822565-2017-05801
Event Type
Injury
Date Received
August 15, 2017
Date of Event
July 13, 2017
Report Date
August 15, 2017
Manufacturer
ZIMMER, INC.
Product Code
JDG
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: UNK, UNKNOWN HEAD, UNK; UNK, UNKNOWN STEM, UNK; UNK, UNKNOWN CUP, UNK. (B)(4). REPORT SOURCE, LITERATURE - MCGRORY, B. ET AL (2017). HIGH EARLY MAJOR COMPLICATION RATE AFTER REVISION FOR MECHANICALLY ASSISTED CREVICE CORROSION IN METAL-ON-POLYETHYLENE TOTAL HIP ARTHROPLASTY. THE JOURNAL OF ARTHROPLASTY, 1-7. DOI: 10.1016/J.ARTH.2017.07.004. 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 - 05798; 0001822565 - 2017 - 05799; 0001822565 - 2017 - 05800. (B)(4).

Description of Event or Problem · 1

IT HAS BEEN REPORTED IN A JOURNAL ARTICLE THAT A PATIENT HAD A LOW TO POOR HARRIS HIP SCORE OF (B)(6). ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
574902 UNKNOWN LINER PROSTHESIS, HIP JDG ZIMMER, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 64 YR Other