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Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Heart Failure/Congestive Heart Failure (4446)
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Event Date 08/07/2023 |
Event Type
Injury
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Event Description
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The manufacturer received information in reference to certain cpap, bipap, and mechanical ventilator devices.The manufacturer received information alleging heart attack.The manufacturer was made aware of this complaint through a representative of the customer.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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Manufacturer Narrative
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Since no device information was provided, the exact recall number is unknown.Possible recall numbers include z-1972-2021, z-1973-2021, and z-1974-2021.H3 other text : device not returned to manufacturer.
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Search Alerts/Recalls
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