FDAJune 23, 2025device

Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941, 10005941J, 10005941JP, 10005941JPN

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Bedside SpO2 Patient Monitoring System alarms not heard/recognized, resulting in: treatment delay, lack of low oxygen saturation response, respiratory failure, arrhythmia. Highlighting operator's manual: 1)For patient Safety don't silence/decrease alarm volume, 2)Sensor off alarm (no perfusion detected) is low priority alarm, 3)Set monitors to Homecare Mode outside of hospital/professional setting

What to do

FDA enforcement status: Ongoing

Brands named

covidien

UPCs

1088452119672810884521163454108845215276071088452117329310884521171534884521512019884521188689

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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