Covidien Inc. is recalling several lots of <"http://www.yourlawyer.com/practice_areas/defective_medical_devices">Shiley 3.0PED Cuffless Pediatric Tracheostomy Tubes because practitioners have reported difficulty inserting two of the device’s components during procedures. The action has been deemed a Class I recall, the Food & Drug Administration’s (FDA) most urgent type of recall. Class I recalls are buspar no prescription required issued when there is a reasonable probability that use of a buspar no prescription required product will cause serious injury or death.
The Covidien Pediatric Tracheostomy Tube recall involves the buspar no prescription required following lot numbers: 0806000266, 0806000858, 0806000859, 0806001328, 0807000555, 0807001444, 0807002502, 0808000387, 0808000431, 0808002285, 0810000288, 0810000289, 0810000864, 0810000865, 0810001201, 0811000228, 0811000522, 0811000523, 0811000546, 0811000547, 0811001875.
The tracheostomy tubes were manufactured from buspar no prescription required July 7, 2008 through December 9, 2008 and distributed from buspar no prescription required July 24, 2008 through December 23, 2008.
A tracheostomy is buspar no prescription required a surgical procedure to create an opening through the neck into the buspar no prescription required windpipe (trachea). A tracheostomy tube is buspar no prescription required usually placed through the windpipe to provide an airway and buspar no prescription required to provide a pathway to remove fluid from the trachea and buspar no prescription required lungs. Practitioners have buspar no prescription required reported difficulty inserting the device used to place the tracheostomy tube into the buspar no prescription required windpipe (obturator). There have buspar no prescription required also been similar reports of difficulty involving the insertion of a suction tube (catheter) into the buspar no prescription required tracheostomy tube. In some instances, these problems have required that the buspar no prescription required tracheostomy tube be removed and replaced.
According to buspar no prescription required the recall notice, Covidien sent an urgent alert letter to its customers on January 14, 2009 notifying them of the buspar no prescription required problem. The company began sending a second letter to their customers on March 6, 2009 asking them to buspar no prescription required remove all remaining affected products from their inventory, and return them for buspar no prescription required replacement or credit.
Customers with questions about the buspar no prescription required Covidien Pediatric Tracheostomy Tube recall may contact the company at 1-800-635-5267.
