FDA Adverse Event Death Summary report: N

UNKNOWN TRAUMA SCREW

MDR report key: 6961598 · Received October 19, 2017

Report

Report Number
0001825034-2017-08921
Event Type
Death
Date Received
October 19, 2017
Report Date
October 26, 2017
Manufacturer
ZIMMER BIOMET, INC.
Product Code
HSB
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). MULTIPLE MDR'S WERE SUBMITTED FOR THIS EVENT. PLEASE SEE REPORTS: 0001825034 - 2017 - 08920. 0001825034 - 2017 - 08921 . 0001825034 - 2017 - 08922. 0001825034 - 2017 - 08923. CONCOMITANT PRODUCTS: UNKNOWN AFFIXUS NAIL. REPORT SOURCE : FOREIGN. THE EVENT(S) OCCURRED IN (B)(6). ¿SURGICAL DELAY AS A RISK FACTOR FOR WOUND INFECTION AFTER A HIP FRACTURE.¿ INJURY, ELSEVIER, 28 SEPT. 2016, WWW.SCIENCEDIRECT.COM/SCIENCE/ARTICLE/PII/S0020138316306076. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. ROOT CAUSE WAS UNABLE TO BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

Additional Manufacturer Narrative · 1

(B)(4). UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED TO NOT BE REPORTABLE AS THIS DEVICE WAS NOT INVOLVED IN THE EVENT. THE INITIAL REPORT WAS SUBMITTED IN ERROR AND SHOULD BE VOIDED.

Description of Event or Problem · 1

FIFTEEN 15 CASES OF CARDIAC FAILURE AS A MORTALITY MEDICAL COMPLICATION WERE REPORTED IN THE STUDY. NO FURTHER INFORMATION HAS BEEN MADE AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
741964 UNKNOWN TRAUMA SCREW ROD, FIXATION HSB ZIMMER BIOMET, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Death| O