FDA Adverse Event Injury Summary report: N

M2A-MAGNUM TAPER INSERT

MDR report key: 9546985 · Received January 3, 2020

Report

Report Number
0001825034-2020-00026
Event Type
Injury
Date Received
January 3, 2020
Date of Event
December 9, 2019
Report Date
April 10, 2020
Manufacturer
ZIMMER BIOMET, INC.
Product Code
KWA
PMA / PMN Number
K042037
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

(B)(4). UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THIS DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE REPORTED EVENT.

Description of Event or Problem · 0

UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THIS DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE REPORTED EVENT.

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: TAPERLOC POR LAT FMRL 11X142 CAT# 11-103205 LOT# 188920, M2A-MAGNUM PF CUP 54ODX48ID CAT# US157854 LOT# 921250, M2A-MAGNUM MOD HD SZ 48MM CAT# 157448 LOT# 721120. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 -2020 -00023, 0001825034 -2020 -00024, 0001825034 -2020 -00025.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL RIGHT HIP ARTHROPLASTY. SUBSEQUENTLY THE PATIENT WAS REVISED APPROXIMATELY 10 YEARS LATER DUE TO PAIN AND ELEVATED METAL ION LEVELS. THE FEMORAL HEAD AND TAPER ADAPTER WERE REMOVED AND REPLACED. 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
5487 M2A-MAGNUM TAPER INSERT PROSTHESIS, HIP KWA ZIMMER BIOMET, INC. NI 060800

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R