Reported Nov 23, 2016 · Terminated
Aptio Automation Modules
Siemens Healthcare Diagnostics, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Siemens Healthcare Diagnostics, Inc. · 500 Gbc Dr Ms 514 · Newark, DE · 19702-2466
Is this the product you have?
- Aptio Automation Modules
- Lot codes and dates
- "Refrigerated
- Storage Module (RSM)
1070304910715227107030361071376210713767"Centrifuge
- Module (CM)
107030321071376110713764"i2000SR
- Interface Module (i2000SR)
1098930310989304
- Amount recalled
- 448 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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