Urgent Recall of Portex Pediatric Tracheal Tubes!
Portex Pediatric Tracheal Tubes were urgently recalled by the U.S Food & Drug Administration and their manufacturer Smiths Medical on September 11, 2009. These tubes, sizes 2.0, 3.0 and 3.5mm, are used in tracheotomies for children, or during surgery in which a tracheal tube is inserted into a child’s windpipe to aid with breathing and removal of secretions.
The recall of Portex Pediatric Tracheal Tubes by the FDA stated that a number of the tubes were manufactured with internal diameters smaller than indicated on the label. This error may cause difficulty clearing secretions from the device or the airway, which may lead to a partial or complete airway obstruction. The product defect may also increase airway resistance and make breathing more difficult. Due to these complications, the FDA recall states, “there is a reasonable probability of serious injury and/or death”.
If your child or someone you know has suffered an airway obstruction injury or death that may be associated with usage of these Portex tracheal tubes, please contact the Pintas Law Firm immediately. Our experienced personal injury attorneys will be able to evaluate your claim. Our Chicago law firm can provide you with a free consultation and an explanation of your legal rights.