FDA Adverse Event Injury Summary report: N

M2A-MAGNUM PF CUP 52ODX46ID

MDR report key: 8343377 · Received February 15, 2019

Report

Report Number
0001825034-2019-00554
Event Type
Injury
Date Received
February 15, 2019
Date of Event
November 2, 2018
Report Date
March 12, 2019
Manufacturer
ZIMMER BIOMET, INC.
Product Code
KWA
PMA / PMN Number
K042037
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

UPON REVIEW OF THE EVENT, IT HAS BEEN DETERMINED THAT THIS EVENT WAS A RESULT OF A COINCIDING PROCEDURE, AND WILL BE REPORTED UNDER MEDWATCH 0001825034-2019-00208. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.

Description of Event or Problem · 0

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

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: 157446 ¿ MAGNUM HEAD ¿ 983620. 15-103203 ¿ TAPERLOC STEM ¿ 571490. 139252 ¿ MAGNUM INSERT ¿ 615460. 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: 0001825034-2019-00556, 0001825034-2019-00557, 0001825034-2019-00558.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT RIGHT HIP REVISION APPROXIMATELY 7 YEARS POST IMPLANTATION. DURING THE PROCEDURE, THE PATIENT EXPERIENCED AN ESTIMATED BLOOD LOSS OF 2800ML, WHICH REQUIRED A BLOOD TRANSFUSION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
135644 M2A-MAGNUM PF CUP 52ODX46ID PROSTHESIS, HIP KWA ZIMMER BIOMET, INC. N/A 849260

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R