ADVIA Centaur® VB12 +C 10330218Recalls & reported problems
Siemens Healthcare Diagnostics Inc. · Vitamin B12 - CENTAUR - RGT - 500 tests · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00630414177175), received between Feb 14, 2018 and Feb 14, 2018 — classified as 1 malfunction.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 14, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE DOCTOR QUESTIONED AN ELEVATED ADVIA CENTAUR XP VITAMIN B12 (VB12) RESULT THAT DID NOT AGREE WITH THE CLINICAL PICTURE OR REPEAT TESTING. THERE ARE NO REPORTS THAT TREATMENT WAS ALTERED OR PRESCRIBED OR ADVERSE HEALTH CONSEQUENCES DUE TO THE ELEVATED ADVIA CENTAUR XP VB12 RESULT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7270721 ↗
Other RADIOASSAY, VITAMIN B12 devices
- Access Vitamin B12 33000Beckman Coulter, Inc. · Radioassay, Vitamin B121 recall16 reports
- ADVIA Centaur® CKMB MCM 10309782Siemens Healthcare Diagnostics Inc. · RADIOASSAY, VITAMIN B121 recall0 reports
- Atellica IM VB12 10995715Siemens Healthcare Diagnostics Inc. · RADIOASSAY, VITAMIN B1224 reports
- Elecsys Vitamin B12 II 07028121190Roche Diagnostics GmbH · RADIOASSAY, VITAMIN B1221 reports
- Atellica IM VB12 10995714Siemens Healthcare Diagnostics Inc. · RADIOASSAY, VITAMIN B1213 reports
- ADVIA Centaur® VB12 10309970Siemens Healthcare Diagnostics Inc. · RADIOASSAY, VITAMIN B128 reports
- ARCHITECT 7K61-37Abbott Ireland · RADIOASSAY, VITAMIN B124 reports
- ARCHITECT 7K61-27Abbott Ireland · RADIOASSAY, VITAMIN B123 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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