FDA Device recall Z-1122-2013
ADVIA Centaur Vitamin D Calibrator 6-pack
- FDA Device
- Class II
- terminated
- Published 2013-04-24
On 2013-04-24 the FDA classified a Class II recall of ADVIA Centaur Vitamin D Calibrator 6-pack by Siemens Healthcare Diagnostics, citing negative bias in patient samples for Vitamin D.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1122-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-03-13 |
| Published | 2013-04-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Healthcare Diagnostics |
| Distribution | US |
Product
ADVIA Centaur Vitamin D Calibrator 6-pack; Reference Number:10630911. For use in the quantitative determination of Vit D.
Reason
Negative bias in patient samples for Vitamin D
Identifiers
| code_info | Lot Number: C3410 Kit Lot Number/Exp. Date: 95010A10 8/16/2013 |
|---|
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-1122-2013%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.