ClearanceBrief
Recall Z-0999-04 ยท JQW Station, Pipetting And Diluting, For Clinical Use

Roche Diagnostics Corp.

Tecan clinical workstation; 10-410 Tecan Genesis 150 back end, Roche catalog number 03585352001.

DateJul 20, 2004 (initiated May 5, 2004)
StatusTerminated
ReasonTecan software has the potential to match the patient with a different patient's test results.
Root causeOther
ActionPress release was issued 5/7/04 and recall letter dated 5/5/04 was sent to user laboratories.
Quantity11
DistributionNationwide. California, Connecticut, Georgia, Illinois, Maryland, Massachusetts, Michigan, New Jersey, Pennsylvania, Tennessee, Texas and Wisconsin.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.