MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2015-05-01 for ADVIA CENTAUR XP manufactured by Siemens Healthcare Diagnostics Inc..
[17585082]
Discordant, (b)(6) results were obtained on two patient sample on an advia centaur xp instrument. The discordant results were not reported to the physician(s). The sample were repeated on an alternate advia centaur xp instrument. The corrected results were reported to the physician(s). There are no reports of patient intervention or adverse health consequences due to the discordant, (b)(6) results.
Patient Sequence No: 1, Text Type: D, B5
[17740087]
A siemens customer service engineer (cse) was dispatched to the customer site. The cse changed the tubing for the sample probe plunger, lubricated the syringe, removed and cleaned the plunger, changed the vertical probe belt, changed the acid and base pumps, and recalibrated the sample probe bottom. The customer is running siemens (b)(6) quality controls every four hours in replicates of ten. The cause of the discordant, (b)(6) result is unknown. The instrument is performing according to specifications. No further evaluation of the device is required.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2432235-2015-00223 |
| MDR Report Key | 4743777 |
| Report Source | 05,06 |
| Date Received | 2015-05-01 |
| Date of Report | 2015-04-07 |
| Date of Event | 2015-04-02 |
| Date Mfgr Received | 2015-04-07 |
| Device Manufacturer Date | 2010-08-30 |
| Date Added to Maude | 2015-06-03 |
| 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 | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | MICHAEL METZ |
| Manufacturer Street | 511 BENEDICT AVENUE |
| Manufacturer City | TARRYTOWN NY 10591 |
| Manufacturer Country | US |
| Manufacturer Postal | 10591 |
| Manufacturer Phone | 9145242223 |
| Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS MANUFACTURING LTD. |
| Manufacturer Street | REGISTRATION NUMBER: 8020888 CHAPEL LANE, SWORDS, CO., |
| Manufacturer City | 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 | OBF |
| Date Received | 2015-05-01 |
| Model Number | ADVIA CENTAUR XP |
| Operator | HEALTH PROFESSIONAL |
| 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 | 2015-05-01 |