FDA Adverse Event Injury Summary report: N

UNKNOWN BI-METRIC COLLARLESS STEM

MDR report key: 7052332 · Received November 22, 2017

Report

Report Number
3002806535-2017-01095
Event Type
Injury
Date Received
November 22, 2017
Report Date
November 22, 2017
Manufacturer
BIOMET UK LTD.
Product Code
JDG
PMA / PMN Number
PNI
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). (B)(6). HUGHES R.E., BATRA A., HALLSTROM B.R. (2017) "ARTHROPLASTY REGISTRIES AROUND THE WORLD: VALUABLE SOURCES OF HIP IMPLANT REVISION RISK DATA.", CURRENT REVIEWS MUSCULOSKELETAL MEDICINE (2017) 10:240¿252, HTTPS://WWW.NCBI.NLM.NIH.GOV/PMC/ARTICLES/PMC5435639/. THE PURPOSE OF THIS PAPER IS TO BRIEFLY DESCRIBE ARTHROPLASTY REGISTRY CONCEPTS, INTERNATIONAL REGISTRIES AROUND THE WORLD, US REGISTRIES, AND PROVIDE A PARSIMONIOUS SUMMARY OF TOTAL HIP ARTHROPLASTY (THA) IMPLANT REVISION RISK REPORTS ACROSS REGISTRIES. THE PRODUCT AND LOT NUMBER IDENTIFICATION NECESSARY TO REVIEW MANUFACTURING HISTORY AND THE COMPLAINT HISTORY WAS NOT PROVIDED. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT CONCLUSION AS TO THE CAUSE OF THE EVENT.

Description of Event or Problem · 1

IT HAS BEEN REPORTED IN A JOURNAL ARTICLE THAT 631 BI-METRIC COLLARLESS STEM AND M2A 38 ONE PIECE CUP (UNCEMENTED IMPLANTS) REVISIONS DUE TO UNKNOWN REASONS WERE PERFORMED. THE DATA WAS OBTAINED FROM THE (B)(6) NATIONAL JOINT REGISTRY FOR THE PAST 10 YEARS. ATTEMPTS HAVE BEEN MADE TO RETRIEVE ADDITIONAL INFORMATION ON THE REPORTED EVENTS, HOWEVER NO INFORMATION HAS BEEN MADE AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
833147 UNKNOWN BI-METRIC COLLARLESS STEM HIP PROSTHESIS JDG BIOMET UK LTD. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R