Skip to content
Recall Observatory FDA recall evidence

Device product

Atellica IM BR 27.29 (BR) Assay 250 Test Kit (Reference)- in vitro diagnostic use in the quantitative serial determination of cancer antigen CA 27.29 in human serum and plasma (EDTA) using the Atellica IM Analyzer.- SMN: 11206236

Z-2426-2021

July 06, 2021

Class II

Product summary

Firm
Siemens Healthcare Diagnostics, Inc
Event
Event 88431
Status
Ongoing
Classification
Class II
Quantity
787 units
Official record key
device-enforcement:Z-2426-2021

Official wording

Reason: Product does not meet the Instructions for Use (IFU) claimed Pack Calibration Interval of 10 days. IFU calibration updated interval from 10 days to 3 days for all current and future kit lot numbers

Code information: All lots impacted Kit lot numbers: 41331255 & 74682255 expiration date 2021-08-03, Lot number: 91605257 expiration date 2021-11-10.

Distribution pattern: Worldwide distribution. US Nationwide, Australia, Bahamas, India, Mexico, Saudi Arabia, and Viet Nam

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Product does not meet the Instructions for Use (IFU) claimed Pack Calibration Interval of 10 days. IFU calibration updated interval from 10 days to 3 days for all current and future kit lot numbers