SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
Report
- Report Number
- 1423500-2011-06503
- Event Type
- Malfunction
- Date Received
- May 25, 2011
- Date of Event
- May 1, 2011
- Report Date
- May 2, 2011
- Manufacturer
- PLASTI ESTERIL, S.A. DE C.V.
- Product Code
- FKX
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MX
- Reporter Occupation
- OTHER
Narratives
(B)(4). THE SAMPLE IS AVAILABLE FOR EVALUATION. A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF BAXTER'S INVESTIGATION, OR IF ANY ADDITIONAL INFORMATION IS RECEIVED. A 510(K) NUMBER WILL NOT BE PROVIDED IN THE EMDR AS THIS PRODUCT IS MANUFACTURED FOR DISTRIBUTION OUTSIDE OF THE U.S. AND DOES NOT HAVE A 510(K) NUMBER. HOWEVER, IT IS BEING REPORTED BECAUSE IT IS THE SAME OR SIMILAR TO THE PRODUCT DISTRIBUTED WITHIN THE U.S.
(B)(4). ONE SAMPLE WERE RECEIVED BY THE MANUFACTURING FACILITY FOR EVALUATION. VISUAL INSPECTION CONFIRMED A SMALL CUT ON THE PRIMARY PACKAGING OF THE TRANSVERSAL SEAL. THE MANUFACTURING FACILITY HAS INDICATED THIS WAS CAUSED BY A FAILURE OF THE PACKAGING MACHINE DURING MANUFACTURING. AN INVESTIGATION WAS CONDUCTED BY THE MANUFACTURING FACILITY AND CORRECTIVE ACTIONS WERE IMPLEMENTED. SIMILAR REPORTS HAVE BEEN RECEIVED; BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED.
THIS IS AN INTERNATIONAL REPORT WHERE A PATIENT IDENTIFIED 1 CASSETTE IN WHICH THE OVERPOUCH WAS BROKEN. THERE WAS NO PATIENT INVOLVEMENT, THE PRODUCT WAS NOT USED. THIS IS REPORT 1 OF 3.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SYSTEM, PERITONEAL, AUTOMATIC DELIVERY | FKX | PLASTI ESTERIL, S.A. DE C.V. | 14SAHC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | HOMECHOICE |