FDA Adverse Event Malfunction Summary report: N

TRIATHLON #7 CR INSERT 11MM

MDR report key: 3002509 · Received March 13, 2013

Report

Report Number
0002249697-2013-00963
Event Type
Malfunction
Date Received
March 13, 2013
Date of Event
February 25, 2013
Report Date
February 25, 2013
Manufacturer
STRYKER ORTHOPAEDICS-MAHWAH
Product Code
JWH
PMA / PMN Number
K040267
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

AN EVALUATION OF THE DEVICE CANNOT BE PERFORMED AS THE DEVICE WAS IMPLANTED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, THE EVALUATION SUMMARY WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

Additional Manufacturer Narrative · 1

THE REPORTED PRODUCT WHICH HAS AN EXPIRY DATE OF 09-2012 (SEPTEMBER 2012) INDICATED ON THE PACKAGING WAS REPORTEDLY USED IN SURGERY ON (B)(6) 2013. IT IS THE RESPONSIBILITY OF THE USER TO VERIFY THE EXPIRATION DATE AND ENSURE THAT THE PRODUCT IS USED WITHIN THIS TIME FRAME. IT IS REPORTED THAT THE SURGEON WAS INFORMED THAT THE PRODUCT WAS EXPIRED AND THE SURGEON DECIDED TO IMPLANT THE PRODUCT IN THE PATIENT ANYWAY. BASED ON THE PROVIDED INFORMATION IT HAS BEEN DETERMINED THAT THIS EVENT IS ASSOCIATED WITH AN OFF-LABEL APPLICATION.

Description of Event or Problem · 1

DURING A KNEE PROCEDURE, THE NURSE TOOK TWO ITEMS FROM A KNEE TRIATHLON KIT WHICH EXPIRY DATE WERE DUE. THE SURGEON WHO WAS ALREADY INFORMED OF THAT SITUATION DECIDED TO IMPLANT THEM IN THE PATIENT.

Description of Event or Problem · 1

DURING A KNEE PROCEDURE, THE NURSE TOOK TWO ITEMS FROM A KNEE TRIATHLON KIT WHICH EXPIRY DATE WERE DUE. THE SURGEON WHO WAS ALREADY INFORMED OF THAT SITUATION DECIDED TO IMPLANT THEM IN THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
104972 TRIATHLON #7 CR INSERT 11MM IMPLANT JWH STRYKER ORTHOPAEDICS-MAHWAH LAW694

Patients

Seq Age Sex Outcome Treatment
1 Other