The worldwide recall comes after the products were found to have an
increased occurrence of being disconnected from the breathing
circuit, resulting in insufficient oxygen supply, the company said.
Teleflex, which said the recall had been labeled as Class I by the
U.S. health regulator, advised patients to immediately discontinue
use of the products and return the affected products.
(Reporting by Saumya Sibi Joseph in Bengaluru; Editing by Shounak
Dasgupta)
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