FDA Adverse Event Injury Summary report: N

TALAR COMPONENT ORANGE SIZE 4 RIGHT

MDR report key: 11139356 · Received January 8, 2021

Report

Report Number
0001822565-2021-00010
Event Type
Injury
Date Received
January 8, 2021
Date of Event
January 24, 2019
Report Date
April 8, 2021
Manufacturer
ZIMMER BIOMET, INC.
Product Code
HSN
UDI-DI
00889024269606
PMA / PMN Number
K120906
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. NO PRODUCT WAS RETURNED OR PICTURES PROVIDED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. REVIEW OF THE DEVICE HISTORY RECORD(S) IDENTIFIED NO DEVIATIONS OR ANOMALIES DURING MANUFACTURING RELATED TO THE REPORTED EVENT. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED. 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.

Description of Event or Problem · 0

NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED. CONCOMITANT MEDICAL DEVICES: TM ANKLE TIBIAL BASE SIZE 4 CAT# 00450004400 LOT# 64199805; PROLONG TIBIAL INSERT SZ 4 +2 CAT# 00450005402 LOT# 63655806; DIST LAT FIB LCK PLATE 6H RT CAT#00-2357-017-06 LOT#NI; P SCR 3 5MMX14MM W/2 7MM HD ST CAT# 00-2348-014-35 LOT#NI - QTY 3; P SCR 3 5MMX16MM W/2 7MM HD ST CAT# 00-2348-016-35 LOT#NI - QTY 2; 3.5MM X 16MM LOCKING SCREW CAT# 00-2359-016-35 LOT#NI; 3.5MM X 18MM LOCKING SCREW CAT# 00-2359-018-35 LOT#NI; 3.5MM X 20MM LOCKING SCREW CAT# 00-2359-020-35 LOT#NI. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001822565 - 2021 - 00009, 0001822565-2020-03873.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN ANKLE PROCEDURE. SUBSEQUENTLY, THE PATIENT HAS REPORTED PAIN AND IMPINGEMENT ISSUES. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
36708 TALAR COMPONENT ORANGE SIZE 4 RIGHT PROSTHESIS, ANKLE HSN ZIMMER BIOMET, INC. NI 63936458 00889024269606

Patients

Seq Age Sex Outcome Treatment
1 Other SEE H10