PlainRecalls
FDA Devices Moderate Class II Terminated

FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation.

Reported: November 23, 2016 Initiated: October 4, 2016 #Z-0587-2017

Product Description

FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation.

Reason for Recall

Inpeco received several notifications from the field about burnt schuko sockets. The customers reported that some smoke was seen coming from the damaged sockets.

Details

Recalling Firm
Inpeco S.A.
Units Affected
188 units
Distribution
Worldwide Distribution - US including Texas and New York. Foreign Consignees: Germany, Italy, France, Austria and Spain.
Location
Lugano, N/A

Frequently Asked Questions

What product was recalled?
FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation.. Recalled by Inpeco S.A.. Units affected: 188 units.
Why was this product recalled?
Inpeco received several notifications from the field about burnt schuko sockets. The customers reported that some smoke was seen coming from the damaged sockets.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 23, 2016. Severity: Moderate. Recall number: Z-0587-2017.