Recall Z-2026-2021

Siemens Healthcare Diagnostics, Inc. · initiated May 13, 2021

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Atellica CH 930 Analyzer - multi-component system for in vitro diagnostic testing of clinical specimens SMN 11067000

Codes / lots: Effected SN Range: CM00902 - CM02065 Note: xxxx in serial number is any number. UDI: 00630414002163

Reason for recall

Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600 analyzers may develop a malfunction due to a manufacturing defect and may result in the valve wearing and leaking over time. The leaking is a risk in valves subject to high pressure or high wear and may impact the result accuracy of any assay.

FDA-determined cause: Component design/selection

Action taken

Siemens issued an Urgent Medical Device Correction (UMDC) ASI21-02.A.US and Urgent Field Safety Notice (UFSN) ASI21-02.A.OUS on 5/13/2021 to all affected customers informing them of the issue and providing instructions the customer must follow until their analyzer is updated with replacement valves that do not have the manufacturing defect. Siemens will release the replacement valves and will begin installation at customer sites in June 2021. Letter states: Actions to be Taken by the Customer The following actions must be taken until your system has been serviced to replace any leaking components. 1. When reporting results, ensure that all QC results are within the laboratory acceptable range before releasing results. A manufacturing defect in some valves may cause them to leak Siemens Healthcare Diagnostics Inc. 2. On the Atellica CH930 Analyzer: If any water droplets are observed on the tips of any Reaction Wash Station or Dilution Wash Station probes, contact Siemens service so that the instrument can be checked for valves that may be failing. 3. On the Atellica IM 1300 or Atellica IM 1600 Analyzers: If any water droplets are observed forming at the tips of any Reagent probes, contact Siemens service so that the instrument can be checked for valves that may be failing. Please review this letter with your Medical Director. Complete and return the Field Correction Effectiveness Check Form attached to this letter within 30 days. If you have received any complaints of illness or adverse events associated with the products listed in Table 1, immediately contact your local Siemens Healthineers Customer Care Center or your local Technical Support representative. Siemens Service representative will be contacting your laboratory to check and replace the identified valves. Please retain this letter with your laboratory records and forward this letter to those who may have received this product. Contact your Siemens Healthineers Customer Care Center or y

Details

Recall number
Z-2026-2021
Initiated
May 13, 2021
Product code
JGS – Electrode, Ion Specific, Sodium
Quantity
US: 210 OUS: 874
Distribution
Nationwide Foreign: Country Name Algeria Argentina Australia Austria Bahrain Bangladesh Belgium Brazil Bulgaria Burkina Faso Canada Chile Colombia Croatia Cura¿ao Cyprus Czech Republic Denmark Ecuador Egypt Estonia Finland France Germany Greece Hungary India Indonesia Iraq Ireland Israel Italy Japan Kenya Kuwait Latvia Libya Lithuania Malaysia Mexico Morocco Netherlands New Zealand Norway Oman…
Recalling firm
Siemens Healthcare Diagnostics, Inc., Tarrytown, NY

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2027-2021 Class IIAtellica IM 1300 Analyzer - multi-component system for in vitro diagnostic testing of…Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600 analyzers may develop a… 05/13/2021Open, Classified
Z-2028-2021 Class IIAtellica IM 1600 Analyzer- multi-component system for in vitro diagnostic testing of…Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600 analyzers may develop a… 05/13/2021Open, Classified