FDA Adverse Event Injury Summary report: N

ECLIPSE CAGE SCREW L, 40MM

MDR report key: 16341666 · Received February 9, 2023

Report

Report Number
1220246-2023-06256
Event Type
Injury
Date Received
February 9, 2023
Date of Event
March 3, 2022
Report Date
August 22, 2024
Manufacturer
ARTHREX, INC.
Product Code
QHQ
UDI-DI
00888867059948
PMA / PMN Number
K183194
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
501

Narratives

Additional Manufacturer Narrative · 0

BASED ON THE INFORMATION PROVIDED WHICH MAY INCLUDE THE DEVICE (IF AVAILABLE AND RETURNED), PICTURES, VIDEOS, EVENT DESCRIPTION, AND ANY ADDITIONAL INFORMATION FROM THE FIELD, ARTHREX WAS ABLE TO CONCLUDE A MOST LIKELY CAUSE. THE REPORTED FAILURE LIKELY STEMS FROM A USE ERROR FOLLOWING THE CORRECT SURGICAL TECHNIQUE FOR THE DEVICE.

Additional Manufacturer Narrative · 0

THE CONTRIBUTION OF THE DEVICE TO THE REPORTED EVENT COULD NOT BE DETERMINED AS THE DEVICE WAS NOT RETURNED FOR EVALUATION. THE ROOT CAUSE OF THE EVENT COULD NOT BE DETERMINED FROM THE INFORMATION AVAILABLE AND WITHOUT DEVICE EVALUATION. IF THE DEVICE BECOMES AVAILABLE FOR EVALUATION, A FOLLOW-UP REPORT WILL BE SUBMITTED.

Description of Event or Problem · 0

ON (B)(6) 2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT WHILE USING AN AR-9301-03 ARTHREX ECLIPSE CAGE SCREW LARGE, AN AR-9400-SBK ECLIPSE SPEEDSCAP IMPLANT SYSTEM AND AN AR-9301-51CPC ECLIPSE TRUNION, DURING THE FINAL STEPS, THE SURGEON DRILLED THE PILOT HOLE INTO THE SCREW AND FIXATION WAS COMPROMISED. SURGEON MOVED TO AN APEX SYSTEM INSTEAD. WHILE USING THE APEX, FIXATION WAS ALSO COMPROMISED WHEN TRAILING THE HEAD, SO SURGEON USED A LARGER SIZE INSTEAD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1358995 ECLIPSE CAGE SCREW L, 40MM TOTAL SHOULDER ARTHROPLASTY SYSTEM QHQ ARTHREX, INC. ECLIPSE CAGE SCREW L, 40MM 22.00817 00888867059948

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Other