Catalog Number NLD-15597-20 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Awareness during Anaesthesia (1707)
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Event Type
Injury
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Manufacturer Narrative
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Customer has not yet returned the device to the manufacturer for device evaluation.When and if the device becomes available and is returned and evaluated the manufacturer will file a follow-up report detailing the results of the evaluation.
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Event Description
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A report was received that stated that a patient received insufficient local anesthesia when the listed medical device was used.It was necessary to place patient under general anesthesia during the procedure.No adverse effects to patient reported.
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Manufacturer Narrative
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The actual sample was not returned for investigation.The supplier of the anaesthesia medication completed a review of manufacturing records for the reported lot and concluded that the product met with specifications at final testing.The supplier also tested retained samples from the same lot for potency.All testing found the product to meet with specifications.
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Search Alerts/Recalls
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