FDA Adverse Event Injury Summary report: N

M2A-T M/H RAD 2HL SHL 37/48MM

MDR report key: 9285416 · Received November 6, 2019

Report

Report Number
0001825034-2019-04972
Event Type
Injury
Date Received
November 6, 2019
Date of Event
September 24, 2019
Report Date
February 13, 2020
Manufacturer
ZIMMER BIOMET, INC.
Product Code
KWA
PMA / PMN Number
K993438
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
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

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

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: 11-163679 188940 28MM M2A HI CARBON HD +3MM NK, 15-105011 560460 M2A TPR HI CARBON 37/28MM LNR, UNKNOWN STEM. REPORT SOURCE: FOREIGN COUNTRY: (B)(6). CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION, DUE TO THE DEVICE WAS DISCARDED. 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 -04975, 0001825034 -2019 -04977.

Description of Event or Problem · 1

IT WAS REPORTED PATIENT UNDERWENT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY 12 YEARS POST IMPLANTATION DUE TO SUSPICION OF PSEUDOTUMOR. 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
1081483 M2A-T M/H RAD 2HL SHL 37/48MM PROSTHESIS, HIP KWA ZIMMER BIOMET, INC. N/A 002150

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R