FDA Adverse Event Injury Summary report: N

UNKNOWN STEM

MDR report key: 8064237 · Received November 13, 2018

Report

Report Number
0001825034-2018-10655
Event Type
Injury
Date Received
November 13, 2018
Report Date
December 4, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
PMA / PMN Number
N/A
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.

Description of Event or Problem · 0

IT WAS REPORTED PATIENT UNDERWENT A LEFT HIP REVISION APPROXIMATELY 8 YEARS POST IMPLANTATION DUE TO UNKNOWN REASONS. THE HEAD COMPONENT WAS REMOVED AND REPLACED, WHILE THE CUP COMPONENT WAS FOUND TO BE WELL FIXED.

Additional Manufacturer Narrative · 1

(B)(4). EVENT DATE (B)(6) 2017. CONCOMITANT MEDICAL PRODUCTS: US157854 - M2A MAGNUM CUP - 790430; 139258 ¿ M2A MAGNUM TAPER INSERT ¿ 916730; 157448 ¿ M2A MAGNUM HEAD ¿ 671350. THERAPY DATE: (B)(6) 2017. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION AS THE PRODUCT LOCATION IS UNKNOWN. 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 EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2018 - 10627; 0001825034 - 2018 - 10629; 0001825034 - 2018 - 10626.

Description of Event or Problem · 1

IT WAS REPORTED PATIENT UNDERWENT A HIP REVISION APPROXIMATELY 8 YEARS POST IMPLANTATION DUE TO UNKNOWN REASONS. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
903131 UNKNOWN STEM PROSTHESIS, HIP JDI ZIMMER BIOMET, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R