ANES CIRCUITS
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
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.
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 |