FDA Adverse Event
Malfunction
Summary report: N
FLOGARD
MDR report key: 3173654
·
Received June 17, 2013
Report
- Report Number
- 1416980-2013-15621
- Event Type
- Malfunction
- Date Received
- June 17, 2013
- Date of Event
- May 9, 2013
- Report Date
- May 23, 2013
- Manufacturer
- BAXTER HEALTHCARE - SINGAPORE
- Product Code
- FRN
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MX
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4). THE DEVICE WAS SERVICED AT THE CUSTOMER SITE. THE DEVICE WAS VISUALLY INSPECTED AND FUNCTIONALLY TESTED. THE REPORTED CONDITION OF DOES NOT WORK WAS CONFIRMED AS A FAILURE 82. THE CAUSE OF THE REPORTED CONDITION WAS DUE TO A DEFECTIVE CENTRAL PROCESSING UNIT (CPU). TO CORRECT THE ISSUE THE CPU WAS REPLACED. THE DEVICE WAS SERVICED AND RESTORED TO A GOOD WORKING CONDITION. IF ANY ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A FOLLOW UP MDR WILL BE SENT.
Description of Event or Problem · 1
IT WAS REPORTED THAT A FLOGARD INFUSION PUMP DOES NOT WORK. THERE WAS NO PATIENT INVOLVEMENT. ADDITIONAL INFORMATION WAS REQUESTED AND IS NOT AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 273656 | FLOGARD | PUMP, INFUSION | FRN | BAXTER HEALTHCARE - SINGAPORE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |