MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2015-02-13 for ADVIA CENTAUR XP 078-A010 manufactured by Siemens Healthcare Diagnostics, Inc..
[5405589]
Discordant vitamin d results were obtained on two patient samples on an advia centaur xp instrument. The initial results were not reported to the physician(s). The samples were repeated on an alternate system. It is unknown which repeat results were reported to the physician(s). There are no known reports of adverse health consequences due to the discordant vitamin d results.
Patient Sequence No: 1, Text Type: D, B5
[12837911]
A siemens customer service engineer (cse) was dispatched to the customer site. After evaluation of the instrument and instrument data, the cse tested the system wash sequence. The cse determined that the aspirate probe 4 assembly was not adequately drawing liquid from the cuvettes. The cse replaced the aspirate probe 4 assembly and successfully ran quality controls. The cause of the discordant vitamin d results is due to an aspirate probe 4 assembly malfunction. The instrument is performing within specifications. Further evaluation of the device is not required.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2432235-2015-00076 |
| MDR Report Key | 4517903 |
| Report Source | 05,06 |
| Date Received | 2015-02-13 |
| Date of Report | 2015-01-19 |
| Date of Event | 2015-01-18 |
| Date Mfgr Received | 2015-01-19 |
| Device Manufacturer Date | 2009-10-08 |
| Date Added to Maude | 2015-03-18 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 0 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 0 |
| Manufacturer Contact | JOHN NELSON |
| Manufacturer Street | 511 BENEDICT AVENUE |
| Manufacturer City | TARRYTOWN NY 10591 |
| Manufacturer Country | US |
| Manufacturer Postal | 10591 |
| Manufacturer Phone | 9145242530 |
| Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS |
| Manufacturer Street | MANUFACTURING LIMITED REGISTRATION NUMBER: 8020888 |
| Manufacturer City | CHAPEL LANE, SWORDS CO DUBLIN, |
| Manufacturer Country | EI |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ADVIA CENTAUR XP |
| Generic Name | IMMUNOASSAY ANALYZER |
| Product Code | MOI |
| Date Received | 2015-02-13 |
| Model Number | ADVIA CENTAUR XP |
| Catalog Number | 078-A010 |
| ID Number | N/A |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS, INC. |
| Manufacturer Address | 511 BENEDICT AVENUE TARRYTOWN NY 10591 US 10591 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2015-02-13 |