Z-0105-2023 Class II Ongoing

Recalled by Siemens Healthcare Diagnostics, Inc. — Tarrytown, NY

Recall Details

Product Type
Devices
Report Date
October 26, 2022
Initiation Date
September 19, 2022
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
586 US; 694 OUS

Product Description

Atellica CH Lithium (Li), Siemens Material Number 11097535. in vitro diagnostic assay

Reason for Recall

Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930 Analyzer. In the worst case, there is a potential for erroneously elevated lithium patient results, which may lead to inappropriate dosage adjustment, potentially affecting treatment efficacy.

Distribution Pattern

Worldwide distribution - US Nationwide.

Code Information

UDI-DI: 00630414006789 All lots impacted: Lots 110354 exp 11/15/22 120038 exp 2/7/23