Model Number 71992-01 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Skin Infection (4544)
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Event Date 02/21/2024 |
Event Type
Injury
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Event Description
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An adverse skin reaction was reported with wear of the adc device.Customer experienced symptoms described as sensor site infection and had contact with an hcp who prescribed antibiotics for treatment.There was no report of death or permanent impairment associated with this event.
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Manufacturer Narrative
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The product has been requested for investigation.A follow-up report will be submitted once additional information is obtained.The date of event 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.
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Manufacturer Narrative
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An extended investigation has been performed for the reported complaint.There was no indication that the product did not meet specification.The reported complaint is related to skin irritation or an allergic reaction to the patch adhesive of the freestyle libre sensor.Dhrs (device history record) for the freestyle libre sensor and freestyle libre sensor kit were reviewed, and the dhrs showed the freestyle libre sensor and freestyle libre sensor kit passed all tests prior to release.Dose audit reports were reviewed and demonstrates the continued effectiveness of the established sterilization process for libre sensor products.Environmental monitoring reports were reviewed, including bioburden and endotoxin testing, and demonstrated that all monitoring processes continue to meet adc minimum requirements for product quality.Sensor (b)(6)as been returned and investigated.No physical damage was observed on the sensor patch.No issues were observed with adhesive.No malfunction or product deficiency was identified.Therefore, the issue is not confirmed. all pertinent information available to abbott diabetes care has been submitted.
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Event Description
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An adverse skin reaction was reported with wear of the adc device.Customer experienced symptoms described as sensor site infection and had contact with an hcp who prescribed antibiotics for treatment.There was no report of death or permanent impairment associated with this event.
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Search Alerts/Recalls
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