Z-0931-2022 Class II Ongoing
FDA device recall Z-0931-2022 was initiated by Siemens Healthcare Diagnostics, Inc. on Feb 9, 2022 and is designated Class II. Reason for recall: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent carryover impacting quality control (QC), patient samples, and calibrator results. The recall status is ongoing. Affected quantity: 2158.
Recall Details
- Product Type
- Devices
- Report Date
- Apr 20, 2022
- Initiation Date
- Feb 9, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2158
Product Description
Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11097637
Reason for Recall
Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent carryover impacting quality control (QC), patient samples, and calibrator results.
Distribution Pattern
Global Distribution. US Nationwide.
Code Information
UDI: 00630414287935; Lot Numbers: 110108 110185 110238 110302
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0931-2022
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026