Data Foundry

Medical device recalls 2023

ADVIA Chemistry ToxAmmonia Calibrator- In vitro diagnostic use in the… — Class II medical device recall Z-1631-2023

Ongoing recall by Siemens Healthcare Diagnostics, Inc., reported 2023-05-31, distributed nationwide. Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA Chemistry ToxAmmonia Calibrators fo

Recall numberZ-1631-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmSiemens Healthcare Diagnostics, Inc., Tarrytown, NY, United States
Recall initiated2023-04-05
Classified2023-05-25
Reported by FDA2023-05-31
DistributedNationwide (US)
Countries outside the USAR, AT, AU, BD, BE, BH, BR, CA, CL, CN, CO, CZ, DE, EE, EG, ES, FI, FR, GR, HK, HU, IL, IN, IT, KR, LV, MX, MY, NL, NO, PK, PL, PT, RS, SE, SK, TR, TW, UY, VN, ZA
Reason classespotency
UPC / GTIN / UDI-DI00630414479286
Lot numbers9520341, 9520531
Expiration dates2023-05-31, 2024-03-31

Product

ADVIA Chemistry ToxAmmonia Calibrator- In vitro diagnostic use in the calibration of ethanol (ETOH_2), ammonia (AMM), acetaminophen (ACET), and salicylate (SAL) assays on the ADVIA¿ Chemistry systems Siemens Material Number (SMN): 10309217

Reason for recall

Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA Chemistry ToxAmmonia Calibrators for the Atellica CH Salicylate (Sal) Assay due to a positive bias

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1631-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.