FDA Adverse Event Malfunction Summary report: N

T4 TOGA, ZIPPER, LARGE/EXTRA LARGE"

MDR report key: 3419447 · Received October 18, 2013

Report

Report Number
0001811755-2013-02568
Event Type
Malfunction
Date Received
October 18, 2013
Date of Event
September 27, 2013
Report Date
September 27, 2013
Manufacturer
STRYKER INSTRUMENTS-KALAMAZOO
Product Code
FYA
PMA / PMN Number
K070078
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE REPORTED EVENT OF FOREIGN MATERIAL IN THE UNOPENED STERILE PACKAGING WAS CONFIRMED BY A MANUFACTURER TECHNICIAN THROUGH VISUAL INSPECTION. IT IS LIKELY THAT THE CAUSE OF THE ISSUE IS A MANUFACTURING ISSUE. SINCE THE DEVICE WAS DESTRUCTIVELY TESTED, IT WAS NOT RETURNED TO THE USER FACILITY.

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION WILL BE SUBMITTED ONCE THE QUALITY INVESTIGATION HAS BEEN PERFORMED.

Description of Event or Problem · 1

IT WAS REPORTED THAT WHEN THE STERILE PACKAGING OF THE HOODS WERE OPENED AT THE USER FACILITY IN PREPARATION FOR A SURGICAL PROCEDURE, A WHITE SUBSTANCE CAME OUT OF THE STERILE PACKAGING. IT WAS REPORTED THAT THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO DELAY, NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT WHEN THE STERILE PACKAGING OF THE HOODS WERE OPENED AT THE USER FACILITY IN PREPARATION FOR A SURGICAL PROCEDURE, A WHITE SUBSTANCE CAME OUT OF THE STERILE PACKAGING. IT WAS REPORTED THAT THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO DELAY, NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
535443 T4 TOGA, ZIPPER, LARGE/EXTRA LARGE" GOWN, SURGICAL FYA STRYKER INSTRUMENTS-KALAMAZOO 13070974

Patients

Seq Age Sex Outcome Treatment
1