FDA Adverse Event Malfunction Summary report: N

OPTIPAC-S 40 REFOBACIN BONE CEMENT R

MDR report key: 5508932 · Received March 17, 2016

Report

Report Number
3006946279-2016-00015
Event Type
Malfunction
Date Received
March 17, 2016
Date of Event
February 17, 2016
Report Date
September 29, 2016
Manufacturer
BIOMET FRANCE S.A.R.L.
Product Code
MBB
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AU
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS USER FACILITY IS OUTSIDE OF THE UNITED STATES. THE NECESSARY MANUFACTURING HISTORY WAS NOT PROVIDED FOR REVIEW. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. THE FOLLOWING SECTIONS COULD NOT BE COMPLETED WITH THE LIMITED INFORMATION PROVIDED: DEVICE INFO - EXPIRATION DATE UNKNOWN. INITIAL REPORTER - NAME UNKNOWN. MANUFACTURE DATE ¿ UNKNOWN. 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 K051496.

Additional Manufacturer Narrative · 1

UPON RECEIPT OF ADDITIONAL INFORMATION, THIS EVENT HAS BEEN DETERMINED TO NOT BE REPORTABLE. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.

Description of Event or Problem · 1

IT WAS REPORTED PATIENT UNDERWENT AN UNKNOWN PROCEDURE ON AN UNKNOWN DATE. DURING THE PROCEDURE WHILE PREPARING THE CEMENT MIXTURE, THE MONOMER LIQUID WOULD NOT DISPENSE AND WOULD NOT ENTER THE CYLINDER. THERE WAS NO PATIENT INJURY AND NO DELAY IN PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
163880 OPTIPAC-S 40 REFOBACIN BONE CEMENT R BONE CEMENT, ANTIBIOTIC MBB BIOMET FRANCE S.A.R.L. N/A A526B17770

Patients

Seq Age Sex Outcome Treatment
1