FDA Adverse Event Injury Summary report: N

UNKNOWN MULLER CUP

MDR report key: 7040501 · Received November 17, 2017

Report

Report Number
3002806535-2017-01041
Event Type
Injury
Date Received
November 17, 2017
Report Date
November 17, 2017
Manufacturer
BIOMET UK LTD.
Product Code
JDI
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). CONCOMITANT MEDICAL PRODUCT - UNKNOWN TAPERLOC STEM, UNKNOWN FEMORAL HEAD. 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. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 3002806535-2017-01040 AND 3002806535-2017-01042.

Description of Event or Problem · 1

IT HAS BEEN REPORTED IN A JOURNAL ARTICLE THAT 441 TAPERLOC STEM AND MULLER CUP (CEMENTED IMPLANTS) REVISIONS FROM THE (B)(6) 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
820111 UNKNOWN MULLER CUP HIP PROSTHESIS JDI BIOMET UK LTD. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R UNKNOWN FEMORAL HEAD| UNKNOWN TAPERLOC STEM