FDA recall record

Tecan Infinite M1000 The Tecan Infinite M1000 is a multifunctional monochromator based recall — FDA Z-2664-2016

The batteries have the potential to overheating, melt or char.

Class IIclassification
Z-2664-2016official record ID
Aug 31, 2016report date

Recall record at a glance

Official recordZ-2664-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTecan US, Inc.
Report dateAug 31, 2016
Recall initiation dateJul 25, 2016
Quantity1 unit
LocationMorrisville, NC, United States

Official product description

Tecan Infinite M1000 The Tecan Infinite M1000 is a multifunctional monochromator based microplate reader that provides high performance for the vast majority of todays microplate applications and research. Besides offering absorbance and fluorescence intensity measurements, the Infinite M1000 allows the measurement of fluorescence polarization and luminescence. The Infinite M1000 is also robotic compatible and offers a built-in stacker option as well as an external injector module. The Infinite M1000 is intended as a general purpose laboratory instrument for professional use, supporting common microplates conforming to the ANSI/SBS standards

Why the product was recalled

The batteries have the potential to overheating, melt or char.

Distribution information

Worldwide Distribution - US including AK, AL, AR, CA, FL, GA, HI, KY, MA, MD, NC, NY, PA, PR, SC, TN, TX, UT, VA. International account: Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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