FDA Adverse Event Injury Summary report: N

TESS HUMERAL REVERSE COROLLA S0

MDR report key: 6114037 · Received November 18, 2016

Report

Report Number
3006946279-2016-00434
Event Type
Injury
Date Received
November 18, 2016
Date of Event
October 19, 2016
Report Date
April 28, 2017
Manufacturer
BIOMET FRANCE S.A.R.L.
Product Code
KWS
PMA / PMN Number
PK060694
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.

Additional Manufacturer Narrative · 1

THE PRODUCT IDENTIFICATION NECESSARY TO REVIEW MANUFACTURING HISTORY WAS NOT PROVIDED. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. (B)(4). THIS USER FACILITY IS OUTSIDE OF THE UNITED STATES. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. 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)(6) MANUFACTURES A SIMILAR DEVICE IN THE UNITED STATES UNDER 510K NUMBER K060694. THIS REPORT IS NUMBER 1 OF 2 MDRS FILED FOR THE SAME PATIENT (REFERENCE 3006946279-2016-00434 / 00435).

Description of Event or Problem · 1

DURING A SHOULDER ARTHROPLASTY, THE HUMERAL INLAY AND COROLLA DID NOT ASSEMBLE AS EXPECTED, AND AS A RESULT THE COROLLA AND HUMERAL INLAY WERE REMOVED AND REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
765072 TESS HUMERAL REVERSE COROLLA S0 PROSTHESIS, SHOULDER KWS BIOMET FRANCE S.A.R.L. N/A 0001098407

Patients

Seq Age Sex Outcome Treatment
1 75 YR Required Intervention