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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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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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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 or heart failure.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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Search Alerts/Recalls
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