Siemens Healthcare Diagnostics, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0590-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Aptio Automation Modules

Product Classification:

Class II

Date Initiated: September 29, 2016

Date Posted: November 23, 2016

Recall Number: Z-0590-2017

Event ID: 75417

Reason for Recall:

Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.

Status: Terminated

Product Quantity: 448 units

Code Information:

"Refrigerated Storage Module (RSM): 10703049, 10715227, 10703036, 10713762, 10713767; "Centrifuge Module (CM): 10703032, 10713761, 10713764; "i2000SR Interface Module (i2000SR): 10989303, 10989304.

Distribution Pattern:

Distributed Nationwide and to the following countries: Australia, Azerbaijan, Bahrain, Bangladesh, Belgium, Brazil, Canada, Czech Republic, Denmark, Egypt, Germany, Greece, Indonesia, Italy, Kingdom Saudi Arabia, Lebanon, Malaysia, P.R. China, Philippines, Portugal, Qatar, Republic Korea, Saudi Arabia, Spain, Sweden, Switzerland, Taiwan, Turkey, U.A.E., United Kingdom, Vietnam

Voluntary or Mandated:

Voluntary: Firm initiated