FDA Adverse Event Other Summary report: N

STRYKER TRITANIUM ACETABULAR SHELL

MDR report key: 23944847 · Received January 2, 2026

Report

Report Number
MW5181595
Event Type
Other
Date Received
January 2, 2026
Date of Event
November 30, 2022
Report Date
December 23, 2025
Manufacturer
STRYKER/ HOWMEDICA OSTEONICS CORP
Product Code
LPH
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
OR, US
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

STRYKER TRITANIUM ACETABULAR SHELL FAILURE WITH CONSEQUENCES OF METALLOSIS, DISABILITY, LOSS OF BUSINESS, ETC. MY HIP WAS REPLACED WITH A STRYKER HIP COMPONENT WHICH FAILED WITHIN A YEAR AND BEGAN CAUSING PAIN, INFLAMMATION AND RAISED METAL LEVELS. REVISION REQUIRED IN (B)(6) OF 2024 WHERE EUGENE SLOCUM SURGEON REPLACED THE FAILED DEVICE AND FOUND DAMAGE FROM METALOSSIS, TISSUE DAMAGE, ETC DUE TO A FAILURE OF THE STRYKER TRITANIUM ACETABULAR SHELL LINING CAUSING METAL ON METAL. I HAVE HAD TO GO ON SSID DISABILITY NOW, BUSINESS LOSS, PAIN, ETC. MY SURGEON (B)(6) WOULD BE MORE THAN PLEASED TO ASSIST WITH ANYTHING HE CAN DO TO GO AFTER STRYKER. HE HAS A NUMBER OF PEOPLE WITH THIS ISSUE AND OTHERS HE KNOWS FROM OTHER SURGEONS THROUGH HIS CONTACT WITH BEING THE PRESIDENT OF AN ORTHOPEDIC ORGANIZATION. THERE IS NO RECALL ON THIS SPECIFIC PART OF THE DEVICE TO MY KNOWLEDGE. THE ENCLOSED DROPBOX SITE GIVES INFORMATION ON THE EXACT ITEM INSTALLED AND THE FAILURE IT DEVELOPED. HTTPS://WWW.DROPBOX.COM/SCL/FO/M79VV9MMLAABJ3IGNWPZQ/ABPDTLKVTS8PZYOJPBGZPJU?RLKEY=LTN0N0VOLSED0PL7VVNRNFDXO&ST=PORU9Q83&DL=0.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
13974 STRYKER TRITANIUM ACETABULAR SHELL PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED LPH STRYKER/ HOWMEDICA OSTEONICS CORP

Patients

Seq Age Sex Outcome Treatment
1 59 YR Female Disability| R| H| O THYROXIN.