Lifesaver Single Patient Use Manual Resuscitator by Teleflex Hudson RCI: Class I Recall – Intake Port Blockage

On May 14, 2015, Teleflex sent an urgent medical device recall letter to customers asking them to immediately discontinue use and quarantine the recalled product. Customers are asked to return any affected product together with a completed Recall Acknowledgement Form, for consolidation and return to Teleflex Medical. The letter also requested a sub-recall of the product through the distributers, instructing them to immediately discontinue distribution and quarantine the recalled products, and notify their customers who have received the product of the recall. [7/2/15]

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