FDA Adverse Event Injury Summary report: N

UNKNOWN JUGGERKNOT

MDR report key: 7346983 · Received March 16, 2018

Report

Report Number
0001825034-2018-01924
Event Type
Injury
Date Received
March 16, 2018
Date of Event
July 21, 2017
Report Date
March 14, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
MBI
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). REPORT SOURCE, LITERATURE - NAKAGAWA, S. ET AL (2017). POSTOPERATIVE RECURRENCE OF INSTABILITY DUE TO NEW ANTERIOR GLENOID RIM FRACTURES AFTER ARTHROSCOPIC BANKART REPAIR. THE AMERICAN JOURNAL OF SPORTS MEDICINE, 45(12), 2840-2848. DOI: 10.1177/0363546517714476. (B)(6). REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. 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. PRODUCT LOCATION UNKNOWN.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT THERE WERE FIFTEEN SHOULDERS WITH POST-OPERATIVE RECURRENCE OF INSTABILITY IN THE SOFT ANCHOR GROUP. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
187211 UNKNOWN JUGGERKNOT FASTENER, FIXATION MBI ZIMMER BIOMET, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention