Reported Oct 31, 2018 · Terminated
APTIO INPUT/OUTPUT MODULE
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. · 511 Benedict Ave · Tarrytown, NY · 10591-5005
Is this the product you have?
- APTIO INPUT/OUTPUT MODULE
- Lot codes and dates
- Siemens Material Numbers
10703031107137601071377510713772
- UDI00630414594477
- Siemens Material Numbers
- Amount recalled
- 441 Aptio Automation Modules
This recall covers 9 products
The agency filed one notice per product. You are reading one of them; the other 8 are below.
Where it was sold
Why it was recalled
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
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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