Siemens Healthcare Diagnostics, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1154-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.
Product Description:

ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10331250 Siemens Material Number (SMN): 10325366

Product Classification:

Class II

Date Initiated: January 9, 2023
Date Posted: March 1, 2023
Recall Number: Z-1154-2023
Event ID: 91522
Reason for Recall:

Negative bias occurred when whole blood calibration (Atellica IM Fol or ADVIA Centaur FolateBA/FolBA) used to test serum samples.

Status: Ongoing
Product Quantity: 124 kits
Code Information:

UDI: (01)00630414454597(10) 16277336(17)20230320; (01)00630414454597(10) 23278336 (17)20230320; (01)00630414454597(10)25958336(17)20230320; (01)00630414454597(10)63092344(17)20230726. Lot Numbers: 16277336, 23278336, 25958336, 63092344 and higher. Affects all current and future lots of the Advia Centaur Folate assay until the Instructions for Use are updated.

Distribution Pattern:

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Voluntary or Mandated:

Voluntary: Firm initiated