Reported Jul 8, 2015 · Terminated

Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…

Tecan US, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Tecan US, Inc. · 9401 Globe Center Drive · Morrisville, NC · 27560

Is this the product you have?

  • Infinite F500, in vitro diagnostic
  • Product UsageThe Tecan Infinite F500 is a multifunctional microplate reader with injector option. The Infinite F500 provides high performance for the vast majority of todays microplate applications and research and is robotic compatible. The Infinite F500 is intended as a general purpose laboratory instrument for professional use, supporting common microplate conforming to the ANS/SBS standards
Lot codes and dates
  • Material Number 30019337. Serial numbers
    • 1212004416
    • 1009002605
    • 612000003
    • 811002510
    • 712004158
    • 906000965
    • 902005109
    • 912003472
    • 1103002583
    • 1411007090
    • 704000003
    • 702000001
    • 708000500
    • 1003004146
    • 1109000103
    • 1412005124
    • 805001219
    • 911005026
    • 708005532
    • 705007195
    • 810000248
    • 1010001663
    • 712004152
    • 708005533
    • 1412005709
    • 1103003780
    • 706004455
    • 608000002
    • 908000185
    • 1009002604
    • 1308001035
    • 804005914
    • 1311007600
    • 804000984
    • 705009034
    • 1309003195
    • 801008055
    • 706007961
    • 901006341
Amount recalled
868 in total

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

A firmware bug causes incorrect values to be displayed for specific measured luminescence values.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 18, 2017 · Data as of Sep 19, 5:27 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.