RecallRadar

FDA Device recall Z-2430-2020

ADVIA Chemistry Calibrator

On 2020-07-01 the FDA classified a Class II recall of ADVIA Chemistry Calibrator by Siemens Healthcare Diagnostics, citing calibration errors have been observed with the Total and Direct Bilirubin assays when using Chemistry Calibrator lot 534177 for ADVIA Chemistry and lot 534179 for Atellica CH.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2430-2020
ClassificationClass II
Statusterminated
Initiated2020-06-05
Published2020-07-01
Last updated2026-09-13 11:55 UTC
CompanySiemens Healthcare Diagnostics
DistributionUS

Product

ADVIA Chemistry Calibrator

Reason

Calibration errors have been observed with the Total and Direct Bilirubin assays when using Chemistry Calibrator lot 534177 for ADVIA Chemistry and lot 534179 for Atellica CH.

Identifiers

code_info
Lots: 534177 (including sublots A, B and C) 960742 UDI: (01)00630414223414(10)534177(17)20210930 (01)00630414223414…Lots: 534177 (including sublots A, B and C) 960742 UDI: (01)00630414223414(10)534177(17)20210930 (01)00630414223414(10)534177A(17)20211031 (01)00630414223414(10)534177B(17)20211231 (01)00630414223414(10)534177C(17)20220131 (01)00630414223414(10)534177D(17)20220331 (01)00630414223414(10)960742(17)20220531

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2430-2020%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.