FDA Adverse Event Injury Summary report: N

TAPERLOC MICROP FMRL 11.0MM

MDR report key: 7395233 · Received April 4, 2018

Report

Report Number
0001825034-2018-02360
Event Type
Injury
Date Received
April 4, 2018
Report Date
April 4, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
PMA / PMN Number
PK050441
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: M2A 38MMX50MM CUP CAT: RD118850 LOT: 792180, M2A 38MM MOD HD +3MM NK CAT: 11-173663 LOT: 601580. REPORTED EVENT WAS CONFIRMED BY REVIEW OF X-RAYS PROVIDED. X-RAY REVIEW STATES ABSENCE OF THE GREATER TROCHANTER AND MILD HETEROTOPIC OSSIFICATION. SMALL INCLINATION ANGLE OF THE ACETABULAR CUP WITH MORE HORIZONTAL ORIENTATION THAN EXPECTED. NO HARDWARE FRACTURE SEEN. POSSIBLE RADIOLUCENCY ALONG THE MEDIAL ACETABULUM AT THE CEMENT HARDWARE INTERFACES. DEVICE HISTORY RECORD WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. 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.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT HAD A LEFT HIP REVISION APPROXIMATELY 12 YEARS POST PRIMARY SURGERY, DUE TO DISLOCATION AND METAL ON METAL REACTION. DURING THE REVISION, THE CUP WAS REPLACED AND TWO SCREWS WERE PUT IN. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
239860 TAPERLOC MICROP FMRL 11.0MM HIP, PROSTHESIS JDI ZIMMER BIOMET, INC. 419280

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R