T4 TOGA, ZIPPER, LARGE/EXTRA LARGE"
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
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 INFORMATION WILL BE SUBMITTED ONCE THE QUALITY INVESTIGATION HAS BEEN PERFORMED.
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.
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 |