The Recall Desk

FDA (Devices) recall action 69739

Tecan US, Inc. recalled 2 products on 2015-01-21

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2015-01-21
Critical
0
Units
8

Why these products were recalled

Incorrect lumi firmware version installed (E.027 instead of V2.00)

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–2 of 2

  • LowFDA (Devices)··2015-01-21

    Tecan Infinite 200 Microplate Reader Recalled for Incorrect Firmware Version

    Tecan US, Inc. is recalling eight Infinite 200 microplate readers because they were shipped with the incorrect lumi firmware version (E.027 instead of V2.00).

    Product
    Infinite 200 The Tecan Infinite 200 is a multifunctional microplate reader with injector option. The Infinite 200 provides high performance for the vast majority of todays microplate applications and research and is robotic compatible. The infinite 200 has been designed as a…
    Category
    Distribution
    1 state
  • LowFDA (Devices)··2015-01-21

    Tecan Infinite 200PRO Microplate Reader Recalled for Firmware Error

    Tecan US, Inc. is recalling Infinite 200PRO microplate readers due to an incorrect firmware version installed on the devices.

    Product
    Infinite 200PRO The Tecan Infinite 200 is a multifunctional microplate reader with injector option. The Infinite 200 provides high performance for the vast majority of todays microplate applications and research and is robotic compatible. The infinite 200 has been designed as…
    Category
    Distribution
    1 state