FDA Adverse Event Malfunction Summary report: N

ENDOTRACHEAL TUBES - AIRWAY MANAGEMENT

MDR report key: 3894570 · Received May 2, 2014

Report

Report Number
9611710-2014-00083
Event Type
Malfunction
Date Received
May 2, 2014
Date of Event
April 7, 2014
Report Date
April 7, 2014
Manufacturer
UNOMEDICAL SDN BHD
Product Code
BTR
PMA / PMN Number
K951696
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

AN EVALUATION WAS PERFORMED ON (B)(4) 2014. RECEIVED WERE 4 UNUSED I.D. 3.0 MM, CATALOG NUMBER: 61130030 ENDOTRACHEAL PLAIN TUBES WITH PP CONNECTORS OF CORRESPONDING SIZE 3.5 MM AND WORK ORDER(B)(4) MARKED AS PER (B)(4) SPECIFICATION. THE SAMPLES WERE TESTED ON (B)(4) 2014. THE SAMPLES WERE INSPECTED AND THE OBSERVATIONS ARE AS FOLLOWS: 1 UNIT SHOWED NO SIGNS OF FOREIGN SUBSTANCE IN PACKAGE, WHERE AS 1 UNIT WAS CONFIRMED FOR HAIR IN PACKAGING, AND 2 UNITS WERE CONFIRMED FOR STAIN ON PRODUCT. REVIEW OF THE ASSEMBLY RECORD DID NOT REVEAL ANY SIGNS OF THE ASSOCIATED DEFECTS DETECTED DURING THE 100% LIGHT TEST. BASED ON THE ANALYSIS OF THE RETURNED SAMPLES PROVIDED IT WAS FOUND THAT 3 OUT OF 4 UNITS RETURNED WERE NOT MEETING OUR INSPECTION CRITERIA. HOWEVER, THIS COMPLAINT ISSUE HAS BEEN INVESTIGATED TO ADDRESS THE CONFIRMED COMPLAINT AND DOCUMENTED IN THE CAPA SYSTEM. NO ADDITIONAL PATIENT/EVENT DETAILS HAVE BEEN PROVIDED TO DATE. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE A FOLLOW-UP REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING INCOMING INSPECTION FOUND "FOREIGN SUBSTANCE IN PACKAGE."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
266260 ENDOTRACHEAL TUBES - AIRWAY MANAGEMENT TUBE, TRACHEAL (W/WO CONNECTOR) BTR UNOMEDICAL SDN BHD 61130030 614639R001

Patients

Seq Age Sex Outcome Treatment
1