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Device Problem
Degraded (1153)
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Patient Problems
Cancer (3262); Solid Tumour (4552)
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Event Date 10/02/2023 |
Event Type
Injury
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Manufacturer Narrative
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Due to the manufacturer not receiving the device information, the following are possible recall z numbers: z-1972-2021, z-1974-2021, z-1973-2021 h3 other text : device not returned to manufacturer.
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Event Description
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The manufacturer was contacted in reference to the voluntary field safety notice/recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.The patient has alleged cancer, carcinoid tumor of lung.Medical intervention was not specified.The device has not yet been returned to the manufacturer for investigation.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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Search Alerts/Recalls
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