FDA Adverse Event Malfunction Summary report: N

ANES CIRCUITS

MDR report key: 2097206 · Received May 11, 2011

Report

Report Number
2242551-2011-00005
Event Type
Malfunction
Date Received
May 11, 2011
Date of Event
April 13, 2011
Report Date
May 11, 2011
Manufacturer
VITAL SIGNS, INC.
Product Code
CAI
PMA / PMN Number
EXEMPT
Removal / Correction Number
224551-04/29/11-004-R
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE HME FILTER WAS RETURNED AND EVALUATED BY GE HEALTHCARE ENGINEERS. SAMPLES FROM IN-HOUSE INVENTORY WERE ALSO DRAWN PER A SAMPLING PLAN AND EVALUATED. IT WAS DETERMINED THAT A PLASTIC MEMBRANE OCCLUDED THE MAJORITY OF THE INTERNAL OPENING OF THE FILTER. THE ROOT CAUSE IS BELIEVED TO BE THAT THE POSITION OF THE MOLD AND THE TORQUE APPLIED TO THE MOLD DURING THE PLASTIC HOUSING MFG WERE NOT SET PROPERLY RESULTING IN A REMNANT PLASTIC MEMBRANE. IT WAS DETERMINED THAT THE PART INSPECTION PROCESS WAS NOT ADEQUATE TO DETECT THIS DEFECT. THE AFFECTED PRODUCTS WERE PLACED ON SHIP HOLD TO CONTAIN THE DEFECT. ALL POTENTIALLY AFFECTED PARTS STILL IN GE HEALTHCARE'S POSSESSION HAVE BEEN REWORKED AND RE-INSPECTED PER A NEW TEST PROCEDURE. GE HEALTHCARE HAS INITIATED A RECALL OF THE POTENTIALLY DEFECTIVE UNITS UNDER CORRECTION / REMOVAL NUMBER: 2242551-04/29/11-004-R. IT WAS DETERMINED DURING EVAL THAT THE FILTER WAS MANUFACTURED SOMETIME BETWEEN 01/12/2011 AND 01/25/2011.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING AN INTERNAL INVENTORY CHECK OF ANES CIRCUITS BY THE SITE, THE 5701 HME FILTER WITHIN AN ANESTHESIA CIRCUIT HAD A PLASTIC MEMBRANE PIECE OCCLUDING THE OPENING. NO PT INVOLVEMENT WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ANES CIRCUITS ANESTHESIA CIRCUIT CAI VITAL SIGNS, INC. A4U52X1X 11090A

Patients

Seq Age Sex Outcome Treatment
1