FDA Adverse Event Malfunction Summary report: N

MALLINCKRODT

MDR report key: 3912446 · Received May 13, 2014

Report

Report Number
2936999-2014-00414
Event Type
Malfunction
Date Received
May 13, 2014
Date of Event
April 1, 2014
Report Date
April 16, 2014
Manufacturer
COVIDIEN
Product Code
BTR
PMA / PMN Number
K090352
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KN
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE SAMPLE ASSOCIATED TO THIS REPORT IS EXPECTED TO BE RETURNED FOR ANALYSIS. IF THE SAMPLE IS RECEIVED, A SUMMARY OF THE INVESTIGATION RESULTS WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.

Description of Event or Problem · 1

CUSTOMER REPORTED, WHILE THE NURSE PROCESSED THE CUFF TEST, SHE FOUND THE AIR LEAKED FROM THE CUFF. CUSTOMER CONFIRMED THAT FAULT WAS IDENTIFIED DURING PRETESTING EFFORTS. NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
285492 MALLINCKRODT TAPERGUARD ORAL/NASAL TRACHEAL TUBE BTR COVIDIEN 13E0577JZX

Patients

Seq Age Sex Outcome Treatment
1