Catalog Number 13546-59S |
Device Problem
Insufficient Information (3190)
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Patient Problem
Blood Loss (2597)
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Event Type
Injury
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Event Description
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It was reported that during a tonsillectomy, the controller was functioning slower and was not coaging vessels as usual.The procedure was completed with the same device and no delay was reported.The patient re-bled in pacu(post-anesthesia care unit).All available information has been disclosed.If additional information should become available, a supplemental report will be submitted accordingly.
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Event Description
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It was reported that during a tonsillectomy, the controller was functioning slower and was not coaging vessels as usual.The procedure was completed with the same device and no delay was reported.The patient re-bled in pacu(post-anesthesia care unit) and was treated with suction cautery to coagulate the bleeding vessels.
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Manufacturer Narrative
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H10: additional information on b5.
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Manufacturer Narrative
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Additional information on d4: serial number (b)(4).H10: h3, h6: the reported device, used in treatment, was received for evaluation.There was no relationship found between the returned device and the reported incident.A visual inspection was performed on the product and observed no issues.A functional evaluation revealed no problems.A review of the device history records show there are no indications to suggest that the product did not meet manufacturing specification or would not be able to perform as intended.A complaint history review found related failures; this failure mode will be trended to assess for any necessary corrective actions.Review of the product instructions for use found adequate warnings and precautions to prevent damage to the device during use.Risk management documents were reviewed finding no additional risks that require to be added to the reference document.No clinical supporting documents were provided to conduct a thorough assessment of the reported issue.Should any additional clinical information be provided this complaint will be re-evaluated.The complaint was not verified and the root cause could not be determined since the reported malfunction could not be duplicated during the product evaluation process.Please select the wand type most appropriate for the procedure.The controller will preset nominal and maximum coblate and coagulation voltages for each wand-style to ensure a safe effective operation.No containment or corrective actions are recommended at this time.There are no indications to suggest that the device/product did not meet specifications upon release into distribution.
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Search Alerts/Recalls
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