FDA Adverse Event Injury Summary report: N

UNK LATARJET PRODUCT

MDR report key: 5990698 · Received September 30, 2016

Report

Report Number
1221934-2016-10411
Event Type
Injury
Date Received
September 30, 2016
Report Date
September 1, 2016
Manufacturer
DEPUY MITEK
Product Code
HWC
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

MITEK MEDICAL SAFETY DEPARTMENT DISCOVERED THIS PUBLISHED WHITE PAPER DETAILING A HISTORICAL EVENT IN WHICH SOME MITEK DEVICES WERE IMPLICATED. IT CANNOT BE CONFIRMED THAT THIS ISSUE HAD BEEN PREVIOUSLY REPORTED TO MITEK, SO AN ADVERSE EVENT REPORT IS BEING FILED TO DOCUMENT THE EXPERIENCE DESCRIBED IN THE ARTICLE. AT THIS POINT IN TIME, NO FURTHER ACTION IS WARRANTED. HOWEVER, THIS FILE WILL REMAINS RECEPTIVE TO ANY POTENTIAL FORTHCOMING INFORMATION RECEIVED THAT IS PERTINENT AND GERMANE TO THIS ISSUE. MITEK WILL CONTINUE TO TRACK ANY RELATED COMPLAINTS WITHIN THIS DEVICE FAMILY AS A MEANS OF MONITORING THE EXTENT WITH WHICH THIS COMPLAINT IS OBSERVED IN THE FIELD.

Additional Manufacturer Narrative · 1

IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. THE LOT EXPIRATION DATE AND PRODUCT CODE IS NOT AVAILABLE CURRENTLY. ASSOCIATED MEDWATCH: 1221934-2016-10412.

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING LITERATURE ARTICLE: GRAFT POSITION AND FUSION RATE FOLLOWING ARTHROSCOPIC LATARJET. AUTHORS: CASABIANCA, LAURENT AND ET AL KNEE SURG SPORTS TRAUMATOL ARTHROSC (2016) 24:507-512 DOI 10.1007/S00167-015-3551-6. N=1 GRAFT FRACTURE DUE TO AN INAPPROPRIATE CORACOID PREPARATION. N=1 EARLY CASE OF OSTEOLYSIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
643193 UNK LATARJET PRODUCT SOFT-TISSUE, ANCHOR, NON-BIOABSORBABLE HWC DEPUY MITEK

Patients

Seq Age Sex Outcome Treatment
1 Other