Data Foundry

Medical device recalls 2016

Infinite 200 PRO The Tecan Infinite 200 PRO is a multifunctional… — Class II medical device recall Z-2663-2016

Terminated recall by Tecan US, Inc., reported 2016-08-31, distributed in AK, AL, AR, CA, FL, GA, HI, KY…. The batteries have the potential to overheating, melt or char.

Recall numberZ-2663-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTecan US, Inc., Morrisville, NC, United States
Recall initiated2016-07-25
Classified2016-08-25
Reported by FDA2016-08-31
Terminated2017-01-23
DistributedAK, AL, AR, CA, FL, GA, HI, KY, MA, MD, NC, NY, PA, PR, SC, TN, TX, UT, VA
Countries outside the USCA
Quantity27 units
Reason classesdevice malfunction
Serial numbers1208002673, 1211001074, 1309006773, 1311008588, 1401006356, 1403000833, 1403003928, 1403005482, 1405000420, 1405002510, 1406009472, 1410002321, 1410004940, 1411008631, 1412005274, 1501008506, 1501008513, 1503001536, 1503002986, 1503004890, 1505009092, 1509001022, 1509008146, 1510004918, 1511009716 and 29 more

Product

Infinite 200 PRO The Tecan Infinite 200 PRO is a multifunctional microplate reader with injector option. The Infinite 200 PRO provides high performance for the vast majority of todays microplate applications and research and is robotic compatible. The Infinite 200 PRO has been designed as a general purpose laboratory instrument for professional use, supporting common 6 to 384-well microplates conforming to the ANSI/SBS standards.

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2663-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.