FDA Adverse Event Injury Summary report: N

UNKNOWN SCREW

MDR report key: 14137675 · Received April 18, 2022

Report

Report Number
0001822565-2022-01119
Event Type
Injury
Date Received
April 18, 2022
Report Date
April 18, 2022
Manufacturer
ZIMMER BIOMET, INC.
Product Code
HWC
PMA / PMN Number
N/A
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TU
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

(B)(4). CAGRI ORS, MD, REMZI CAYLAK, MD, EMRE TOGRUL, MD. (16 JUNE 2021). TOTAL HIP ARTHROPLASTY WITH THE WAGNER CONE FEMORAL STEM IN PATIENTS WITH CROWE IV DEVELOPMENTAL DYSPLASIA OF THE HIP: A RETROSPECTIVE STUDY, 37 (2022) 103-109. HTTPS://DOI.ORG/10.1016/J.ARTH.2021.09.007. FOREIGN REPORT SOURCE: (B)(6). NO PRODUCT WAS RETURNED OR PICTURES PROVIDED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. MEDICAL RECORDS WERE NOT PROVIDED. PART AND LOT IDENTIFICATION ARE NECESSARY FOR REVIEW OF DEVICE HISTORY RECORDS, NEITHER WERE PROVIDED. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT 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. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001822565 - 2022 ¿ 00597, 0001822565 - 2022 - 01117, 0001822565 - 2022 - 01118.

Description of Event or Problem · 0

IT WAS REPORTED IN A JOURNAL ARTICLE THAT THREE (3) PATIENTS UNDERWENT ACETABULAR REVISIONS DUE TO ASEPTIC LOOSENING. NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2626391 UNKNOWN SCREW PROSTHESIS, HIP HWC ZIMMER BIOMET, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Unknown Hospitalization| R UNKNOWN HEAD| UNKNOWN LINER| UNKNOWN STEM