Centurion Medical Products and FDA notified healthcare professionals about a Class I recall of Premie Pack, Kit Code LM 110 and Full Term Meconium Pack, Kit Code LM115. The pediatric tracheal tubes used in these kits were manufactured with an internal diameter smaller than indicated on the label, which could result in an inability to remove secretions and cause partial or complete blockage of the airway and the inability to ventilate the patient. These products were distributed from January 1, 2007 through September 22, 2009.
Centurion Medical Products Premie Pack and Meconium Pack Recall*Posted by Healthcare Packaging on November 17, 2009 | PermalinkFiled in: FDA, regulatory and legal; Medical devices Related ArticlesRevivexxx Extra Strength: Recall - Undeclared Drug Ingredient | Aug 09, 2010 Solo Slim, Solo Slim Extra Strength: Recall - Undeclared Drug Ingredient | Aug 09, 2010 June 2010 Drug Safety Labeling Changes: 28 Medical Product Labels with changes | Aug 04, 2010
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