FDA Adverse Event Injury Summary report: N

UNKNOWN HIP

MDR report key: 6936624 · Received October 10, 2017

Report

Report Number
0001825034-2017-08280
Event Type
Injury
Date Received
October 10, 2017
Report Date
October 9, 2017
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NL
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). REPORTED EVENT WAS UNABLE TO BE CONFIRMED AS PART NUMBER AND LOT NUMBER OF THE DEVICE INVOLVED IN THE INCIDENT IS UNKNOWN. DEVICE HISTORY RECORD 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 AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. 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. BOSKER, B.H. ¿PSUEDOTUMOR FORMATION AND SERUM IONS AFTER LARGE HEAD METAL-ON-METAL STEMMED TOTAL HIP REPLACEMENT. RISK FACTORS, TIME COURSE AND REVISIONS IN 706 HIPS.¿ ARCH ORTHOP TRAUMA SURG, VOL. 10, NO. 1007, SER. 00402-015-2165-2, 24 OCT. 2014. 00402-015-2165-2.

Description of Event or Problem · 1

INFORMATION WAS RECEIVED BASED ON REVIEW OF A JOURNAL ARTICLE TITLED, "PSEUDOTUMOR FORMATION AND SERUM IONS AFTER LARGE HEAD METAL-ON-METAL STEMMED TOTAL HIP REPLACEMENT. RISK FACTORS, TIME COURSE AND REVISIONS IN 706 HIPS". THIS ARTICLE IDENTIFIED PATIENTS THAT HAD HIP REVISIONS POST TOTAL HIP ARTHROPLASTY (THA) DUE TO PSEUDOTUMORS. THERE HAS BEEN NO FURTHER INFORMATION PROVIDED AND THE PATIENT OUTCOME IS UNKNOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
717174 UNKNOWN HIP HIP PROSTHESIS JDI ZIMMER BIOMET, INC. N/A UNK

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R