medical Class II Updated 2021-03-31

CAIRE DIAGNOSTICS INC recalls CAIRE DIAGNOSTICS FenomPro REF 900-0001 SN ***** - Product U

Recalled 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.


Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All units sold before February 23, 2021 are affected (serial numbers 100107 to 100651).
View official government recall

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