CELL-DYN 3200 CS 110V ANALYZER
Report
- Report Number
- 2919069-2011-00537
- Event Type
- Malfunction
- Date Received
- August 5, 2011
- Date of Event
- July 8, 2011
- Report Date
- May 17, 2011
- Manufacturer
- ABBOTT DIAGNOSTICS DIVISION
- Product Code
- GKZ
- PMA / PMN Number
- K972354
- Removal / Correction Number
- 2919069-3/15/11-001-C
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IT
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
THIS REPORT IS A DUPLICATE REPORT AND WAS PREVIOUSLY REPORTED UNDER REPORT NUMBER 2919069-2011-00526.
(B)(4): DEVICE MISASSEMBLED DURING MANUFACTURING OR SHIPPING. AN EXPANDED INVESTIGATION WAS CONDUCTED TO EVALUATE THIS ISSUE. A PRODUCT CORRECTION LETTER AND CUSTOMER REPLY FORM WILL BE SENT TO ALL ACTIVE CELL-DYN SYSTEM CUSTOMERS WHO RECEIVED THE AFFECTED PART NUMBERS. THE PRODUCT CORRECTION LETTER WILL INSTRUCT CUSTOMERS TO RETURN THE CUSTOMER REPLY FORM TO ABBOTT ACKNOWLEDGING THE RECEIPT AND UNDERSTANDING THE ISSUE OR REQUEST ASSISTANCE. THE NON-CONFORMING PARTS WILL BE REPLACED IN THE FIELD THROUGH A FOUR-MONTH MANDATORY TECHNICAL SERVICE BULLETIN (TSB) ISSUED FOR EACH OF THE CELL-DYNS INVOLVED.
ON THE INITIAL MEDWATCH 3500A REPORT, MFR RECEIVED DATE WAS UNINTENTIONALLY LEFT BLANK. THE DATE ENTERED SHOULD HAVE BEEN (B)(4) 2011.
THE CUSTOMER HAD THE CELL-DYN SHEAR VALVE DRIVER ASSEMBLY REPLACED PER FA15MAR2011. NO IMPACT TO PATIENT RESULTS, PATIENT MANAGEMENT OR USER SAFETY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CELL-DYN 3200 CS 110V ANALYZER | GKZ | ABBOTT DIAGNOSTICS DIVISION |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | SHEAR VALVE DRIVER |