BIVONA® ADULT TTS¿ HYPERFLEX¿ TRACHEOSTOMY TUBE
Report
- Report Number
- 3012307300-2019-06309
- Event Type
- Injury
- Date Received
- November 11, 2019
- Date of Event
- October 19, 2019
- Report Date
- November 11, 2019
- Manufacturer
- SMITHS MEDICAL ASD; INC.
- Product Code
- JOH
- UDI-DI
- 15021312013818
- PMA / PMN Number
- K081440
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TW
- Reporter Occupation
- OTHER
Narratives
ONE BIVONA® ADULT TTS¿ HYPERFLEX¿ TRACHEOSTOMY TUBE WAS RETURNED FOR ANALYSIS. VISUAL INSPECTION REVEALED A BLACK PIECE OF TAPE WAS FOUND ON THE CUFF AND TWO MARKS ON THE CUFF. THE CUFF WAS THEN INFLATED WITH AIR BUT WAS OBSERVED TO DEFLATE WITHIN ONE MINUTE. THE DEVICE WAS THEN PUT THROUGH LEAK TESTING; THE LEAK WAS FOUND TO BE LEAKING NEAR THE RIGHT SIDE OF THE TAPE. MAGNIFICATION WAS USED TO INSPECT THE CUFF; ABRASIONS WERE FOUND ON THE CUFF. BASED ON THE EVIDENCE THE COMPLAINT WAS CONFIRMED. THE ROOT CAUSE WAS FOUND TO BE USER INTERFACE AS THE ABRASIONS WERE LIKELY DUE TO REPOSSESSING.
INFORMATION WAS RECEIVED INDICATING THAT 10 DAYS FOLLOWING PLACEMENT OF A SMITHS MEDICAL BIVONA® ADULT TTS¿ HYPERFLEX¿ TRACHEOSTOMY TUBE THE VENTILATOR WAS ALARMING AND 3MLS OF WATER WAS REMAINING IN THE CUFF. IT WAS REPORTED THAT INITIALLY 8MLS OF STERILE WATER WAS USED TO INFLATE THE CUFF. THE PHYSICIAN HAD DECIDED TO USE THIS TYPE OF TRACH AS THE PATIENT HAD A TRACHEOMALACIA. SUBSEQUENTLY, A TRACH TUBE CHANGE OUT WAS PERFORMED. A PINHOLE ON THE CUFF WAS FOUND FOLLOWING REMOVAL. THERE WERE NO REPORTED ADVERSE PATIENT EFFECTS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1100886 | BIVONA® ADULT TTS¿ HYPERFLEX¿ TRACHEOSTOMY TUBE | TUBE TRACHEOSTOMY AND TUBE CUFF | JOH | SMITHS MEDICAL ASD; INC. | 3789980 | 15021312013818 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |