FDA recall Z-1230-2020

Siemens Healthcare Diagnostics, Inc. · Class II · device

Product

ADVIA Chemistry Enzymatic Creatinine (ECRE_2) reagent, SMN 10335869

Reason for recall

There is a potential for falsely depressed creatinine results for patients on phenindione therapy when using the enzymatic methodology. Interference has not been observed with the creatinine Jaffe methodology.

Distribution

US Nationwide

Key facts

Status
Terminated
Initiation date
2019-12-18
Report date
2020-02-26
Termination date
2020-06-25
Voluntary/Mandated
Voluntary: Firm initiated
Location
Tarrytown, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1230-2020