Philips flags new problems with previously-replaced ventilators

The FDA said the company had notified it that the sound abatement foam could come loose in some refurbished models, "lowering the inspiratory pressure".

Published On 2022-11-21 03:30 GMT   |   Update On 2022-11-21 11:38 GMT
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Amsterdam: Philips, which has been struggling with a major recall of ventilators, on Monday flagged further problems with some machines it has previously replaced, according to an FDA statement.

A Philips spokesperson said that only Trilogy 100/200 venilator models were potentially affected.

The FDA said the company had notified it that the sound abatement foam could come loose in some refurbished models, "lowering the inspiratory pressure".

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In addition, trace amounts of particulate matter were found in the air pathways of some reworked ventilators.

Read also: Philips expanded ventilator recall classified as most serious by USFDA

Philips has replaced more than 4 million ventilators and sleep apnoea machines over the past 18 months due to worries that the foam used in the machines could become toxic.

The spokesperson said Trilogy 100/200 ventilators represent around 3% of the recall, and no sleep apnoea machines were affected.

Philips shares declined 1.3% to 13.55 euros in Amsterdam.

Read also: Philips recalls some masks used with respiratory devices over safety issues

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Article Source : Reuters

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