Reported Nov 6, 2013 · Terminated
Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic imaging
Toshiba American Medical Systems 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: Toshiba American Medical Systems Inc · 2441 Michelle Dr · Tustin, CA · 92780-7047
Is this the product you have?
- Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic imaging
- Lot codes and dates
- Lot Numbers not utilized
- Serial Numbers
431 of 431 codes
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
- Amount recalled
- 430 (1352 total)
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
The firm initiated this recall of certain Toshiba Diagnostic Ultrasound Systems because it has been found that under certain conditions, the temperature of the transducer head may increase in 2D+PW mode or 2D+CDI (POWER, ADF) +PW mode. When the system is used under both conditions listed below, the temperature of the transducer head connected to the system may increase in temperature and possibly
This product could cause temporary or reversible health problems — stop using it.
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