The U.S. Food and Drug Administration, on Wednesday, classified the recall of certain tubes made by a unit of ICU Medical as the most serious type, which could cause severe injury or death.
Smiths Medical has recalled and removed Bivona neonatal/pediatric and adult tracheostomy tubes due to a manufacturing defect that can cause the securement flange of the device to tear, which can cause ...
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19, 2024 /PRNewswire/ -- Smiths Medical issued an Urgent Medical Device Notification on May 29, 2024, to notify affected customers of a potential issue with certain Bivona ® Tracheostomy Tubes.