FDA Adverse Event Malfunction Summary report: N

ANKLE LOCKING NAIL 12 X 210MM

MDR report key: 12696597 · Received October 26, 2021

Report

Report Number
0001825034-2021-02947
Event Type
Malfunction
Date Received
October 26, 2021
Date of Event
September 26, 2021
Report Date
November 17, 2021
Manufacturer
ZIMMER BIOMET, INC.
Product Code
HSB
PMA / PMN Number
K091976
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. THE FOLLOWING SECTIONS WERE CORRECTED: H6 (HEALTH EFFECT - IMPACT CODE). RADIOGRAPHS WERE PROVIDED AND REVIEWED BY A HEALTH CARE PROFESSIONAL. REVIEW OF THE AVAILABLE RECORDS IDENTIFIED THE FOLLOWING: DISPLACEMENT OF THE NAIL END CAP AT THE CALCANEUS. NO FRACTURE OR OTHER ABNORMALITY IS NOTED AND ALIGNMENT IS MAINTAINED. A SMALL AMOUNT OF RADIOLUCENCY IS NOTED ALONG THE DISTAL NAIL AND END CAP. 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). REPORT SOURCE FOREIGN: (B)(6). CONCOMITANT MEDICAL PRODUCTS: OFFSET END CAP 11X10MM .433D OFFSET CAT: 14-440072 LOT: 773890R. TI-DBLE LEAD CORT 5.0X28MM SCR CAT: 14-405028 LOT: 101720. TI-DBLE LEAD CORT 5.0X28MM SCR CAT: 14-405028 LOT: 907050. TI-DBLE LEAD CORT 5.0X46MM SCR CAT: 14-405046 LOT: 916480. TI-DBLE LEAD CORT 5.0X75MM SCR CAT: 14-405075 LOT: 729800R. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL RIGHT ANKLE PROCEDURE. SUBSEQUENTLY, THE IMPLANTS DISASSEMBLED. NO REVISION PROCEDURE HAS BEEN INDICATED AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1596550 ANKLE LOCKING NAIL 12 X 210MM ROD, FIXATION HSB ZIMMER BIOMET, INC. 028130

Patients

Seq Age Sex Outcome Treatment
1 Male SEE H10