FDA Adverse Event Injury Summary report: N

ELEOS

MDR report key: 15298727 · Received August 25, 2022

Report

Report Number
3013450937-2022-00224
Event Type
Injury
Date Received
August 25, 2022
Date of Event
July 26, 2022
Report Date
November 23, 2022
Manufacturer
ONKOS SURGICAL
Product Code
KRO
UDI-DI
B278KSP10100E0
PMA / PMN Number
K161520
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE INVESTIGATION IS IN PROGRESS. WHEN IT IS COMPLETE A SUPPLEMENTAL MDR WILL BE SUBMITTED ACCORDINGLY. MULTIPLE MDRS WERE SUBMITTED FOR THIS ADVERSE EVENT: 3013450937-2022-00220, 3013450937-2022-00221, 3013450937-2022-00222, 3013450937-2022-00223, 3013450937-2022-00225, 3013450937-2022-00226 AND 3013450937-2022-00227.

Additional Manufacturer Narrative · 0

THIS REPORT IS BEING SUBMITTED TO INCLUDE ADDITIONAL INFORMATION. THE INVESTIGATION IS COMPLETE. THE DEVICE WAS NOT RETURNED FOR EVALUATION. THE ROOT CAUSE OF THE ALLEGED INFECTION COULD NOT BE DETERMINED. ON 24 OCT 2022, WHEN COMPLETING THE INVESTIGATION, IT WAS IDENTIFIED THAT TWO OF THE INITIAL MDRS THAT WERE SUBMITTED DID NOT SUCCESSFULLY GO THROUGH AS THEY WERE ASSIGNED DUPLICATE MFR NUMBERS. 3013450937-2022-00349 AND 3013450937-2022-00348 WERE SUBMITTED FOR THESE PARTS. MULTIPLE MDRS WERE SUBMITTED FOR THIS ADVERSE EVENT: 3013450937-2022-00348, 3013450937-2022-0000349, 3013450937-2022-00222, 3013450937-2022-00223, 3013450937-2022-00225, 3013450937-2022-00226 AND 3013450937-2022-00227.

Description of Event or Problem · 0

IT WAS REPORTED THAT A PATIENT EXPERIENCED AN INFECTION AND UNDERWENT A REVISION SURGERY. THE FOLLOWING IMPLANTS WERE REMOVED DURING THE REVISION: ELEOS DISTAL FEMUR AXIAL PIN, ELEOS TIBIAL BASEPLATE, ELEOS TIBIAL POLY SPACER, ELEOS TIBIAL HINGE W/ ROTATIONAL STOP, ELEOS STEM EXTENSION, ELEOS DISTAL FEMUR, ELEOS TIBIAL BLOCK AUGMENT AND ELEOS CEMENTED SEGMENTAL STEM.

Description of Event or Problem · 0

IT WAS REPORTED THAT A PATIENT EXPERIENCED AN INFECTION AND UNDERWENT A REVISION SURGERY. THE FOLLOWING IMPLANTS WERE REMOVED DURING THE REVISION: ELEOS DISTAL FEMUR AXIAL PIN, ELEOS TIBIAL BASEPLATE, ELEOS TIBIAL POLY SPACER, ELEOS TIBIAL HINGE W/ ROTATIONAL STOP, ELEOS STEM EXTENSION, ELEOS DISTAL FEMUR, ELEOS TIBIAL BLOCK AUGMENT AND ELEOS CEMENTED SEGMENTAL STEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1828839 ELEOS STEM EXTENSION, CANAL FILLING SIZE:11MM X 100M, STRAIGHT, SPLINED, SLOTTED KRO ONKOS SURGICAL KSP10100E 1752007 B278KSP10100E0

Patients

Seq Age Sex Outcome Treatment
1 73 YR Female Hospitalization| R 25000009E ELEOS DISTAL FEMUR SIZE:RIGHT, SEGMENTAL| 25001208E ELEOS TIBIAL POLY SPACER THICKNESS: 8MM| 25002111E ELEOS DISTAL FEMUR AXIAL PIN| CS-13120-03M ELEOS CEMENTED SEGMENTAL STEM| KTAGB210E ELEOS TIBIAL BLOCK AUGMENT SIZE: 2| TB-2202E-01M ELEOS SIZE 2 TIBIAL BASEPLATE| THSMWRS01M ELEOS TIBIAL HINGE W/ROTATIONAL STOP