FDA Device Intelligence
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Test, System, Immunoassay, Lipoprotein-Associated Phospholipase A2

FDA product code NOE · Class 2 · Immunology

3
Registered devices
1
Adverse events
12
Recalls
8
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2010-08-20DiaDexus, IncProduct fails stability tests prior to expiration date.
2010-03-15DiaDexus, IncThe reason for the recall is that Real Time Stability Test program showed the kit lot failed stability prior to expiration, affecting samples with results> 500
2009-10-29DiaDexus, IncInaccurate results-- some samples may return with falsely elevated results potentially as a result of an interfering substance. Some patients may be subjected
2009-10-29DiaDexus, IncInaccurate results-- some samples may return with falsely elevated results potentially as a result of an interfering substance. Some patients may be subjected
2009-10-29DiaDexus, IncInaccurate results-- some samples may return with falsely elevated results potentially as a result of an interfering substance. Some patients may be subjected
2009-10-29DiaDexus, IncInaccurate results-- some samples may return with falsely elevated results potentially as a result of an interfering substance. Some patients may be subjected
2009-10-29DiaDexus, IncInaccurate results-- some samples may return with falsely elevated results potentially as a result of an interfering substance. Some patients may be subjected
2009-10-29DiaDexus, IncInaccurate results-- some samples may return with falsely elevated results potentially as a result of an interfering substance. Some patients may be subjected
2009-02-09DiaDexus, IncPremature Expiration-- the product is projected to fall short of expected shelf life, and may result in inaccurate results.
2008-11-04DiaDexus, IncStorage equipment failure at distributor site due to Hurricane Ike caused product to experience a temperature variation and go out of range. The integrity of t

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.