FDA Adverse Event Injury Summary report: N

BIVONA® ADULT TTS¿ HYPERFLEX¿ TRACHEOSTOMY TUBE

MDR report key: 9306144 · Received November 11, 2019

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

Additional Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

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