Device product
CAIRE DIAGNOSTICS FenomPro REF 900-0001 SN ***** - Product Usage: a portable, non-invasive device to measure fractional exhaled nitric oxide (FeNO) in human breath. Fenom Pro should not be used in critical care, emergency care or in anesthesiology.
Z-1284-2021
Product summary
- Event
- Event 87445
- Status
- Terminated
- Classification
- Class II
- Quantity
- 381 units (171 units U.S. and 210 units O.U.S.)
- Official record key
device-enforcement:Z-1284-2021
Official wording
Reason: Erroneously high FeNO levels which may contribute to premature discontinuation of effective asthma treatment and persistent underlying disease. Two issues affecting the FeNO readings: 1) Drift in the calibration gases and 2) Software error. Each of these issues can cause FeNO scores/results to be erroneously high.
Code information: All units sold before February 23, 2021 are affected (serial numbers 100107 to 100651).
Distribution pattern: Worldwide distribution - U.S. Nationwide distribution in the states of CA, CO, FL, TX, and WI. In the countries of Belgium, Canada, Croatia/Hrvatska, France, Germany, Greece, Hong Kong, India, Philippines, Spain, Spain and Switzerland.
Derived failure modes
-
Device software or design
Software error