FDA Adverse Event Injury Summary report: N

ORTHOPAEDIC SALVAGE SYSTEM 7CM SEGMENTAL FEMORAL COMPONENT RIGHT

MDR report key: 17552844 · Received August 15, 2023

Report

Report Number
0001825034-2023-01898
Event Type
Injury
Date Received
August 15, 2023
Date of Event
July 21, 2023
Report Date
December 19, 2023
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
UDI-DI
00880304238824
PMA / PMN Number
K002757
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. H6 - COMPONENT CODE - PROPOSED CODE IS MECHANICAL (G04) - FEMORAL. THE DEVICE HISTORY RECORDS WERE REVIEWED AND NO DISCREPANCIES WERE IDENTIFIED. A DEFINITIVE ROOT CAUSE COULD NOT BE DETERMINED WITH THE INFORMATION 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.

Additional Manufacturer Narrative · 0

(B)(4). D10 - CONCOMITANT DEVICES - ORTHOPAEDIC SALVAGE SYSTEM POLY LOCK PIN CATALOG #: 150478 LOT #: 395950, ORTHOPAEDIC SALVAGE SYSTEM 4CM DIAPHYSEAL SEGMENT CATALOG #: 150482 LOT #: 640430, ORTHOPAEDIC SALVAGE SYSTEM CEMENTED IM STEM 15MM X 150MM CATALOG #: 150369 LOT #: 055900, ORTHOPAEDIC SALVAGE SYSTEM MODULAR TIBIAL BASEPLATE 79MM CATALOG #: 150424 LOT #: 689560, SERIES A 3 PEG PATELLA THIN 37MM X 8.6MM CATALOG #: 184788 LOT #: 277320, ORTHOPAEDIC SALVAGE SYSTEM POLYETHYLENE TIBIAL BEARING 16MM CATALOG #: 150412 LOT #: 622440, ORTHOPAEDIC SALVAGE SYSTEM REINFORCED YOKE CATALOG #: 150493 LOT #: 293580, ORTHOPAEDIC SALVAGE SYSTEM POLYETHYLENE FEMORAL BUSHINGS CATALOG #: 150477 LOT #: 096430, ORTHOPAEDIC SALVAGE SYSTEM AXLE CATALOG #: 150480 LOT #: 942420, ORTHOPAEDIC SALVAGE SYSTEM POLYETHYLENE TIBIAL BUSHING CATALOG #: 150476 LOT #: 540910. THE COMPLAINANT HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION, AS THE DEVICES WERE DISCARDED. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS PATIENT; PLEASE SEE ALL REPORTS ASSOCIATED WITH THIS EVENT: 0001825034-2023-01892, 0001825034-2023-01896, 0001825034-2023-01897, 0001825034-2023-01898, 0001825034-2023-01899, 0001825034-2023-01900, 0001825034-2023-01901, 0001825034-2023-01903, 0001825034-2023-01904, 0001825034-2023-01905 & 0001825034-2023-01906. H3 : INVESTIGATION INCOMPLETE.

Description of Event or Problem · 0

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

Description of Event or Problem · 0

IT WAS REPORTED THAT THE PATIENT UNDERWENT A RIGHT KNEE ARTHROPLASTY REVISION TO ADDRESS POST-OPERATIVE INSTABILITY AND BONE PRESERVATION. ATTEMPTS HAVE BEEN MADE, HOWEVER, NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1198176 ORTHOPAEDIC SALVAGE SYSTEM 7CM SEGMENTAL FEMORAL COMPONENT RIGHT PROSTHESIS, KNEE JDI ZIMMER BIOMET, INC. N/A 782310 00880304238824

Patients

Seq Age Sex Outcome Treatment
1 Male Required Intervention| H SEE H10 NARRATIVE