FDA Adverse Event Injury Summary report: N

RINGLOC-X E1 H/W 60/36MM 26

MDR report key: 5809989 · Received July 20, 2016

Report

Report Number
3002806535-2016-00562
Event Type
Injury
Date Received
July 20, 2016
Date of Event
June 30, 2013
Report Date
August 22, 2016
Manufacturer
BIOMET UK LTD.
Product Code
LPH
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS FOLLOW-UP REPORT IS BEING FILED TO RELAY ADDITIONAL INFORMATION, WHICH WAS UNKNOWN AT THE TIME OF THE INITIAL MEDWATCH.

Additional Manufacturer Narrative · 1

THIS USER FACILITY IS OUTSIDE OF THE UNITED STATES. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. THE NECESSARY MANUFACTURING HISTORY WAS NOT PROVIDED FOR REVIEW. THIS PRODUCT IS MANUFACTURED BY ZIMMER BIOMET (B)(4) AND IS NOT CLEARED OR DISTRIBUTED IN THE U.S. HOWEVER, THIS REPORT IS BEING SUBMITTED AS ZIMMER BIOMET IN (B)(4), MANUFACTURES A SIMILAR DEVICE IN THE UNITED STATES UNDER 510K NUMBER K023357. THE FOLLOWING SECTIONS COULD NOT BE COMPLETED WITH THE LIMITED INFORMATION PROVIDED: DEVICE CODE - EXPIRATION DATE NI. INITIAL REPORTER - NAME NI. THIS REPORT IS NUMBER 1 OF 4 MDRS FILED FOR THE SAME PATIENT (REFERENCE 3002806535-2016-00562 / 00563 & 1825034-2016-02658 / 02659).

Description of Event or Problem · 1

IT WAS REPORTED THAT PATIENT ENROLLED IN A CLINICAL STUDY AND UNDERWENT A RIGHT CLOSED REDUCTION PROCEDURE APPROXIMATELY TWENTY-FOUR DAYS POST-IMPLANTATION DUE TO LUXATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
463098 RINGLOC-X E1 H/W 60/36MM 26 PROSTHESIS, HIP LPH BIOMET UK LTD. N/A 2841624

Patients

Seq Age Sex Outcome Treatment
1 58 YR Required Intervention