FDA Adverse Event Injury Summary report: N

UNKNOWN CERAMIC HEAD

MDR report key: 6778047 · Received August 9, 2017

Report

Report Number
3002806535-2017-00637
Event Type
Injury
Date Received
August 9, 2017
Date of Event
November 3, 2016
Report Date
August 8, 2017
Manufacturer
BIOMET UK LTD.
Product Code
LZO
PMA / PMN Number
PNI
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). BORGWARDT, A. ET AL (2016) A RANDOMISED, CONTROLLED CLINICAL STUDY ON TOTAL HIP ARTHROPLASTY USING 4 DIFFERENT BEARINGS: RESULTS AFTER 10 YEARS. HIP INTERNATIONAL 2017; 27 (1): 96-103. DOI: 10.5301/HIPINT.5000428. REPORT SOURCE, FOREIGN - EVENT OCCURRED IN (B)(6). 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.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE, 16 PATIENTS IN GROUP D EXPERIENCED 1 OR MORE DISLOCATION OF HIP PROSTHESIS. IT IS UNKNOWN IF THESE PATIENTS UNDERWENT INTERVENTION. NO FURTHER INFORMATION HAS BEEN PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
560022 UNKNOWN CERAMIC HEAD PROSTHESIS, HIP LZO BIOMET UK LTD. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Other