Draeger Initiates a Voluntary Device Recall of Stabilet: Contacts Current Users
MedSun: Newsletter #39, August 2009

Recall - Firm Press Release

Draeger Medical and FDA notified healthcare professionals that it recommends the removal of Stabilet Infant Warmer models 200, 300, 1250, 1500, 200/3000, 2000, 2200/3200, 3000, and 3200 from service as soon as possible due to concern that continued use of these devices may result in serious injury to the patient and/or caregiver.

Additional Information:

Recall – Firm Press Release. Dräger Initiates a Voluntary Device Recall of Stabilet: Contacts Current Users. July 20, 2009.
http://www.fda.gov/Safety/Recalls/ucm172783.htm

Firm Recall Notice. Dräger Initiates a Voluntary Device Recall of Stabilet: Contacts Current Users. July 20, 2009.

http://www.draeger.com/media/10/03/20/10032012/pr_090720_43us_stabilet.pdf

FDA MedWatch Safety Alert. Stabilet Infant Warmer models 200, 300, 1250, 1500, 200/3000, 2000, 2200/3200, 3000, and 3200 [Dräeger/Hill-Rom]. July 20, 2009.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm173239.htm


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