Model Number 71953-01 |
Device Problem
Power Problem (3010)
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Patient Problem
Hypoglycemia (1912)
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Event Date 07/17/2022 |
Event Type
Injury
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Manufacturer Narrative
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The customer¿s product has been requested for investigation.A follow-up report will be filed once additional information is obtained.The device manufacturing date is unknown.The date entered is the date abbott diabetes care became aware of the event.All pertinent information available to abbott diabetes care has been submitted.
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Event Description
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A customer reported a delivery issue associated with a replacement adc device.The customer initially reported experiencing an unspecified battery/power issue with the adc device and a replacement was issued.The customer indicated that due to receiving the incorrect device (freestyle libre 14 day reader instead of freestyle libre 2 reader) they were unable to set glucose alarms, as the function is not available for the freestyle libre 14 day reader.Due to this, the customer became hypoglycemic and required treatment of cola, carbohydrates, and glucose provided by a third-party.There was no report of death or permanent injury associated with this event.
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Manufacturer Narrative
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Repeated attempts by adc to retrieve the product were unsuccessful and/or the customer discarded the product.No product has been returned and a valid serial number has not been provided.Extended investigation has been performed for the reported complaint and there was no indication that the product did not meet specification.A tripped trend review was conducted for the reported complaint and libre reader, no trends were identified that would indicate any product related issues.If the product is returned, a physical investigation will be performed and a follow-up report submitted.All pertinent information available to abbott diabetes care has been submitted.
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Event Description
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A customer reported a delivery issue associated with a replacement adc device.The customer initially reported experiencing an unspecified battery/power issue with the adc device and a replacement was issued.The customer indicated that due to receiving the incorrect device (freestyle libre 14 day reader instead of freestyle libre 2 reader) they were unable to set glucose alarms, as the function is not available for the freestyle libre 14 day reader.Due to this, the customer became hypoglycemic and required treatment of cola, carbohydrates, and glucose provided by a third-party.There was no report of death or permanent injury associated with this event.
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Search Alerts/Recalls
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