The actual complaint product was not returned for evaluation.A review of the device history record is in-progress.All information reasonably known as of 02 apr 2024 has been included in this health authority report.Should additional information be obtained, a follow-up health authority report will be provided.The information provided by avanos medical inc.Represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant reporter was unable or unwilling to provide any further patient, product, or procedural details to avanos medical inc.Avanos medical inc.Has no independent knowledge of the reported event but is relaying the information provided by the user facility where the incident occurred.This product incident is documented in the avanos medical complaint database and identified as complaint : (b)(4).This information is submitted pursuant to 21cfr803, in compliance with the medical device reporting requirement and should not be considered to be an admission that an avanos medical inc.Product is defective or caused serious injury.
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It was reported, ¿last week when i was inserting the percutaneous endoscopic gastrostomy (peg) once the guidewire had been brought back out of the patient¿s mouth it snapped in half.We had to take the wire out, open a new peg pack and rescoped the patient to pass another wire through the trocar and bring it back up through the patient¿s mouth.¿ no injury occurred to the patient.
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