MIC* TJ FEEDING TUBE KIT 18 FR, 45CM (ENDO/RADIOL)
Report
- Report Number
- 9611594-2015-00132
- Event Type
- Malfunction
- Date Received
- August 5, 2015
- Date of Event
- July 22, 2015
- Report Date
- September 17, 2015
- Manufacturer
- HALYARD HEALTH
- Product Code
- KGC
- PMA / PMN Number
- PK080253
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
UDI # UNKNOWN. THE DEVICE HISTORY RECORD FOR THE REPORTED LOT NUMBER, AA4230N12, WAS REVIEWED AND DOCUMENTED THAT THE LOT WAS MANUFACTURED ACCORDING TO THE APPROVED MANUFACTURING PROCEDURES, SPECIFICATIONS, AND THEN RELEASED BY QUALITY ASSURANCE. HALYARD HEALTH HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. THIS PRODUCT INCIDENT IS DOCUMENTED IN THE HALYARD HEALTH COMPLAINT DATABASE AND IDENTIFIED AS COMPLAINT (B)(4).
(B)(4). UPON COMPLETION OF THE INVESTIGATION; A FOLLOW-UP REPORT WILL BE FILED. HALYARD HEALTH HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. THIS PRODUCT INCIDENT IS DOCUMENTED IN THE HALYARD HEALTH COMPLAINT DATABASE AND IDENTIFIED AS COMPLAINT (B)(4). DEVICE NOT RETURNED.
IT WAS REPORTED THAT THE TRANSJEJUNAL FEEDING TUBE INITIALLY PLACED ON (B)(6) 2015 DEVELOPED A TEAR DOWN THE JEJUNAL PORTION OF THE TUBE. THE TRANSJEJUNAL TUBE WAS REPLACED WITHOUT FURTHER INCIDENT. NO PATIENT INJURY REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 517042 | MIC* TJ FEEDING TUBE KIT 18 FR, 45CM (ENDO/RADIOL) | DH EF BALLOON TUBES PRODUCTS | KGC | HALYARD HEALTH | 0250-18 | AA4230N12 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 85 YR |