FDA Adverse Event Injury Summary report: N

32MM MOD HEAD COCR STD NECK

MDR report key: 7531395 · Received May 21, 2018

Report

Report Number
0001825034-2018-03093
Event Type
Injury
Date Received
May 21, 2018
Date of Event
April 23, 2018
Report Date
August 8, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
PMA / PMN Number
PK911684
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
EI
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). IMPLANT DATE - (B)(6) 2018. CONCOMITANT MEDICAL PRODUCTS: 51-101100, TPRLC 133 FP TYPE1 PPS HO 10.0, 6104976, 163669, 32MM MOD HEAD COCR STD NECK, J6070741, 010000665, G7 PPS LTD ACET SHELL 56F, 6209960, 010000928, G7 HI-WALL E1 LINER 32MM F, 6180830. REPORT SOURCE, FOREIGN - THE EVENT OCCURRED IN (B)(6). CUSTOMER HAS INDICATED THAT THE PRODUCT IS IN PROCESS OF BEING RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. 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 - 03092.

Additional Manufacturer Narrative · 1

UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE AS THERE IS NO FAILURE ALLEGED AGAINST THE DEVICE. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED TWO MONTHS POST-IMPLANTATION DUE TO DISLOCATION. THE STEM SANK WITHIN THE FEMUR. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
371896 32MM MOD HEAD COCR STD NECK PROSTHESIS, HIP JDI ZIMMER BIOMET, INC. N/A J6070741

Patients

Seq Age Sex Outcome Treatment
1 78 YR Hospitalization| R