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[Recalled] Aptio Automation Modules — Possible overheating of power cord plugs used to connect to FlexLab and Aptio A… | FDA 2016-09-29

recall fda device united-states

Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.

Recall details

ProductAptio Automation Modules
Brand / manufacturerSiemens Healthcare Diagnostics, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0590-2017
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date29 September 2016
EAN / barcode10703049

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Siemens Healthcare Diagnostics, Inc.

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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