News Releases

February 14, 2012

Salter Labs Recalls 7600 Bubble Humidifier Used with Supplemental Oxygen Therapy

The Missouri Department of Health and Senior Services received the following recall regarding Salter Labs 7600 Bubble Humidifier because the lids fail to pop off at the intended pressure.  When the pop-off occurs, the brass slug does not always reseat to the appropriate position. When the slug fails to reseat properly, the humidifier can leak. A humidifier leak will potentially interrupt the flow of supplemental oxygen to the patient. Hypoxemia may develop resulting in death or serious adverse health consequences.

Special order patient kits were sold under the following brand names:

AUDIENCE: Home Care, Consumers

The 7600 Bubble Humidifier is used for supplemental oxygen therapy. The humidifier is used to provide additional humidity to supplemental oxygen therapy. This product is a single-use device used in health care facilities and home health care. Model numbers include 7600-0-50, E7600-0-50, NP7600-0-50 and special order patient kits that contain 7600 bubble humidifiers. Lot numbers: 091911 and 092611.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

The full recall announcement can be found at:  www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm291820.htm?source=govdelivery.

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