FDA Device recall Z-0173-2014
ADVIA Centaur Intact PTH Calibrator (6 pack)
- FDA Device
- Class III
- terminated
- Published 2013-11-13
On 2013-11-13 the FDA classified a Class III recall of ADVIA Centaur Intact PTH Calibrator (6 pack) by Siemens Healthcare Diagnostics, citing PTH Calibrator packaged with only high calibrator.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0173-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-08-16 |
| Published | 2013-11-13 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Healthcare Diagnostics |
| Distribution | US |
Product
ADVIA Centaur Intact PTH Calibrator (6 pack); Catalog Number: SMN 10492387 For in vitro diagnostic use in calibrating Intact PTH assays on the ADVIA Centaur Systems.
Reason
PTH Calibrator packaged with only high calibrator.
Identifiers
| code_info | Kit Lot: 14136A16 04 Mar 2014 |
|---|
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-0173-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.