Model Number 75175-83 |
Device Problem
Battery Problem (2885)
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Patient Problem
Insufficient Information (4580)
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Event Date 09/05/2022 |
Event Type
Injury
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Event Description
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A customer reported being unable to test using the adc device due to a fast draining battery.As a result, the customer reported requiring unspecified healthcare professional treatment.No further treatment was required.
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Manufacturer Narrative
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At this time product has not yet been returned and a valid serial number has not been provided.An extended investigation has been performed for the reported complaint and it has been determined that there was no indication that the product did not meet specification.A tripped trend review was conducted for the reported complaint and fs libre reader and 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.The date the incident occurred 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 being unable to test using the adc device due to a fast draining battery.As a result, the customer reported requiring unspecified healthcare professional treatment.No further treatment was required.
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Manufacturer Narrative
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At this time product has not yet been returned and a valid serial number has not been provided.An extended investigation has been performed for the reported complaint and it has been determined that there was no indication that the product did not meet specification.A tripped trend review was conducted for the reported complaint and fs optium neo meter and 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.The date the incident occurred is unknown.The date entered in section b3 is the date abbott diabetes care became aware of the event.All pertinent information available to abbott diabetes care has been submitted.This serves as a correction report.Updated section h10 with correct product name.
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Search Alerts/Recalls
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