Skip to content
Recall Observatory FDA recall evidence

Device product

Genesys Analytical Column, REF 01-05-0017 intended to be used with automated high performance liquid chromatography (HPLC) systems employing ion exchange chromatography. For in vitro diagnostic use only.

Z-0621-2019

November 01, 2018

Class II

Product summary

Firm
Clark Laboratories, Inc. (dba,Trinity Biotech USA)
Event
Event 81488
Status
Terminated
Classification
Class II
Quantity
372 units
Official record key
device-enforcement:Z-0621-2019

Official wording

Reason: lack of 510K

Code information: all serial numbers

Distribution pattern: IL, WV, NJ, AZ, MD, UT

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    lack of 510K