Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2661-2016 — 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 physiolog

U.S. FDA — Device Enforcement · United States · 2016-07-25 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2661-2016
Date of alert: 2016-07-25
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Tecan US, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 16039400

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Related