Model Number DS560HS |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problem
Pharyngitis (2367)
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Event Date 02/01/2024 |
Event Type
malfunction
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Event Description
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The manufacturer received information in relation to a remstar auto a-flex unit.The patient alleged that his throat and nose are dry and suspected that this incident is associated with the usage of the device.There was no allegation of serious or permanent harm or injury.No medical intervention was required for the patient.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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H3 other text : device not returned to manufacturer.
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Manufacturer Narrative
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The manufacturer received information from hong kong in relation to a remstar auto a-flex unit.The patient alleged that his throat and nose are dry and suspected that this incident is associated with the usage of the device.There was no allegation of serious or permanent harm or injury.No medical intervention was required for the patient.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.In this report, these sections: describe event or problem (b5) and reporter country have been updated.
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Event Description
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The manufacturer received information from hong kong in relation to a remstar auto a-flex unit.The patient alleged that his throat and nose are dry and suspected that this incident is associated with the usage of the device.There was no allegation of serious or permanent harm or injury.No medical intervention was required for the patient.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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