Aptio Automation Modules
Reported: November 23, 2016 Initiated: September 29, 2016 #Z-0590-2017
Product Description
Aptio Automation Modules
Reason for Recall
Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.
Details
- Recalling Firm
- Siemens Healthcare Diagnostics, Inc.
- Units Affected
- 448 units
- Distribution
- 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
- Location
- Newark, DE
Frequently Asked Questions
What product was recalled? ▼
Aptio Automation Modules. Recalled by Siemens Healthcare Diagnostics, Inc.. Units affected: 448 units.
Why was this product recalled? ▼
Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 23, 2016. Severity: Moderate. Recall number: Z-0590-2017.
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