FDA pegs Edwards Lifesciences Sapien
delivery system recall as severest
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[August 23, 2019]
(Reuters) - The U.S. health regulator on
Thursday categorized the recall of Edwards Lifesciences Corp's Sapien 3
Ultra delivery system as extremely serious, highlighting health risks
associated with its use, but the products will remain on the market.
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The system is used to deliver and deploy a transcatheter heart valve
to replace a diseased aortic valve without open-heart surgery.
In July, the medical device maker sent a safety notice to customers
and doctors, recommending that the balloon in the delivery system be
inflated slowly and continuously when deploying the heart valve to
avoid rupture.
The company said it is not pulling the delivery system from the
market, but rather has issued updated instructions for use to its
customers.
The Food and Drug Administration uses the term "recall" when a
manufacturer takes a corrective action or removes a problematic
medical device from the market. A recall does not always mean that
customers must stop using the product or return it to the company.
The agency said balloons that have burst during implantation
procedures resulted in significant difficulty in retrieving the
valve into the catheter and withdrawing the system from a patient's
body. (https://bit.ly/2MzmXuG)
Edwards started taking action in July after receiving reports of 17
injuries and one death.
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The recall affects 1,585 heart valve delivery systems, the FDA said.
However, Edwards said the recall was immaterial to the company's
revenue forecast.
The FDA's decision to classify the issue as a Class I recall, its
most severe, should not be viewed as a new issue or an escalation of
the problem, rather it is an acknowledgement of its severity,
Jefferies analyst Raj Denhoy said in a note.
Last week, the company's Sapien 3 And Sapien 3 Ultra heart valves
were approved by the agency for use in patients at low-risk of death
linked to such surgeries.
(Reporting by Manojna Maddipatla in Bengaluru; Editing by Shinjini
Ganguli, Bernard Orr)
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