FDA Device recall Z-0859-2015
ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests
- FDA Device
- Class II
- terminated
- Published 2014-12-31
On 2014-12-31 the FDA classified a Class II recall of ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests by Siemens Healthcare Diagnostics, citing A slight crack of the tubing at the connecting fitting on the reservoir connector assembly may occur due to mechanical stress.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0859-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-09 |
| Published | 2014-12-31 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Healthcare Diagnostics |
| Distribution | US |
Product
ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.
Reason
A slight crack of the tubing at the connecting fitting on the reservoir connector assembly may occur due to mechanical stress.
Identifiers
| code_info | Product Codes: 10284980, 10286140, 10309524, 10309525, 10310210, 10313282, 10314322, 10316248, 10316372, 10316968, 1031…Product Codes: 10284980, 10286140, 10309524, 10309525, 10310210, 10313282, 10314322, 10316248, 10316372, 10316968, 10317060, 10317403, 10319111, 10319433, 10320929, 10321568, 10322149, 10322731, 10323204, 10325015, 10326217, 10327008, 10327379, 10328250, 10328647, 10329364, 10330873, 10331013, 10332617, 10334139, 10334759, 10337512, 10337526, 10339677, 10340551, 10340737, 10341051, 10341110, 10361010, 10361011 and 10361012 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0859-2015%22
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