SUNRISE instrument — Class II medical device recall Z-2661-2016
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 number | Z-2661-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Tecan US, Inc., Morrisville, NC, United States |
| Recall initiated | 2016-07-25 |
| Classified | 2016-08-25 |
| Reported by FDA | 2016-08-31 |
| Terminated | 2017-01-23 |
| Distributed | AK, AL, AR, CA, FL, GA, HI, KY, MA, MD, NC, NY, PA, PR, SC, TN, TX, UT, VA |
| Countries outside the US | CA |
| Quantity | 19 units |
| Reason classes | device malfunction |
| Serial numbers | 1201008596, 1403008116, 1404001455, 1404001456, 1405002373, 1405003467, 1407000866, 1409007597, 1412005606, 1503003902, 1504004857, 1504007122, 1506006286, 1509005071, 1511009478, 1512005969, 1603000018, 1606001263, 1606001277, 2CE3362777, 2CE3461RV1, 2CE3461RVY, 2CE3462FX0, 2CE41503MD, 2CE4220BW9 and 13 more |
Product
SUNRISE instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light absorbance (optical density) of liquid media. The instrument is intended to be used primarily in in-vitro diagnostic analysis of samples from the human body to obtain information on physiological and pathological states. For applications in human clinical diagnostic uses, only the Magellan Tracker software is intended for the use with the instrument. Software and instrument have been validated for measurement and for the evaluation of qualitative and quantitative Enzyme-linked Immunosorbent Assays (ELISA) according to the scheduled diagnostic parameters and instrument specifications; they are therefore for professional use in in-vitro diagnostics
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-2661-2016. 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.