Gyrus ACMI Micron Bobbin Vent Tube T: Class I Recall
MedSun: Newsletter #47, April 2010

FDA MedWatch Safety Alert

FDA and Gyrus ACMI notified healthcare professionals of a Class I recall of Gyrus ACMI Micron Bobbin Vent Tube T, 1.27 mm. Units of the product in lot number MH136952 have been shipped without being sterilized. This product was manufactured only on December 17, 2009 and distributed only on December 22, 2009. Patients should contact their physicians to discuss symptoms that may result from use of the affected products.

Additional Information:

FDA MedWatch Safety Alert. Gyrus ACMI Micron Bobbin Vent Tube T: Class I Recall. March 17, 2010.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204992.htm