| Subject: | FDA Announces Class I Recall of Respironics, Inc., SmartMonitor 2 Infant Apnea Monitor |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 18 May 2009 - 05:00 pm |
| The Food and Drug Administration (FDA) is informing healthcare professionals of a Class I Recall of two Respironics, Inc., SmartMonitor 2 Infant Apnea Monitors (Models 4002 and 4003 with serial numbers 3000033364 through 3000038740). This device, used for the continuous monitoring of respiration and heart rate of infant patients in the home or in the hospital, detects and alarms for periods of central apnea or low heart rates. The monitors are being recalled because the devices may... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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