Tecan U S Inc Tecan Clinical Workstations with Robonet software Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Tecan Clinical Workstations with Robonet software
Brand
Tecan U S Inc
Lot Codes / Batch Numbers
PN 10-410 Tecan Genesis 150/8 Back End Configuration, PN 10-415 Tecan Genesis 150/8 Front End Configuration, PN 10-309 Tecan Genesis 200/8 Workstation, PN 10-307 Tecan Genesis 150/8 Workstation, PN 10-043A Tecan Genesis RSP 150/8, PN 10-040A Tecan Genesis RSP 100/4, PN 10-401A Tecan Genesis RSP 100/8
Products Sold
PN 10-410 Tecan Genesis 150/8 Back End Configuration, PN 10-415 Tecan Genesis 150/8 Front End Configuration, PN 10-309 Tecan Genesis 200/8 Workstation, PN 10-307 Tecan Genesis 150/8 Workstation, PN 10-043A Tecan Genesis RSP 150/8, PN 10-040A Tecan Genesis RSP 100/4, PN 10-401A Tecan Genesis RSP 100/8,
Tecan U S Inc is recalling Tecan Clinical Workstations with Robonet software due to Tecan software has the potential to match the patient with a different patient's test results.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Tecan software has the potential to match the patient with a different patient's test results.
Recommended Action
Per FDA guidance
Consignees were notified by letter on May 3, 2004
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, CT, GA, IL, IN, MD, MA, MI, NJ, NY, PA, TN, TX, VA, WI
Page updated: Jan 10, 2026