HUDSON COMFORT FLO PLUS CANNULA W/CHIN STRAP-M
Report
- Report Number
- 8040412-2017-00014
- Event Type
- Malfunction
- Date Received
- January 6, 2017
- Date of Event
- December 20, 2016
- Report Date
- December 22, 2016
- Manufacturer
- TELEFLEX MEDICAL
- Product Code
- CAT
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NC, US
- Reporter Occupation
- RESPIRATORY THERAPIST
Narratives
(B)(4). THE INVESTIGATION INTO THIS COMPLAINT IS STILL IN PROGRESS.
(B)(4). CORRECTED DATA: CATALOG# CORRECTED TO 2412-13. THE SAMPLE WAS RETURNED FOR EVALUATION. A VISUAL EXAM WAS PERFORMED AND IT WAS OBSERVED THAT THERE WAS A HOLE IN THE TUBE. IT IS POSSIBLE THAT THIS DEFECT OCCURRED DUE TO MISHANDLING OF THE PRODUCT. THE FAILURE WAS REPORTED DURING USE ON A PATIENT. THE TUBE MUST BE SOFT AND FLEXIBLE IN ORDER TO MEET THE HFNC OXYGEN THERAPY AND USER REQUIREMENT; THUS IT IS PRONE TO TEARS AND PIN HOLES WHEN IT IS OVER PULLED AND STRETCHED. THE INSTRUCTIONS FOR USE (IFU) MENTIONS THAT THE TUBING SHOULD NOT BE STRETCHED TO REMOVE CONDENSATION, OR DAMAGE/MALFUNCTION MAY OCCUR. IN THE CURRENT MANUFACTURING PROCEDURE, 100% LEAK TESTING IS CONDUCTED DURING THE ASSEMBLY PROCESS AND 100% VISUAL INSPECTION IS DONE AT THE PACKING AREA. ANY DEFECTIVE PRODUCTS WOULD BE DETECTED PRIOR TO RELEASE FROM THE MANUFACTURING FACILITY.
CUSTOMER COMPLAINT ALLEGES "TUBING ON THE CANNULA HAS HOLES." ALLEGED DEFECT DETECTED DURING USE. NO HARM OR INJURY TO THE PATIENT. PATIENT CONDITION REPORTED AS "FINE".
CUSTOMER COMPLAINT ALLEGES "TUBING ON THE CANNULA HAS HOLES." ALLEGED DEFECT DETECTED DURING USE. NO HARM OR INJURY TO THE PATIENT. PATIENT CONDITION REPORTED AS "FINE".
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 11353 | HUDSON COMFORT FLO PLUS CANNULA W/CHIN STRAP-M | CANNULA, NASAL OXYGEN | CAT | TELEFLEX MEDICAL | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |