Model Number PM050 |
Device Problem
Material Integrity Problem (2978)
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Patient Problem
Foreign Body In Patient (2687)
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Event Date 07/03/2022 |
Event Type
malfunction
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Event Description
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Avanos medical inc.Received a single report that referenced two different incidences, which were associated with separate units, involving two different patients.This is the first of two reports.Refer to 2026095-2022-00085 for the second report.It was reported, during removal of the on-q soaker catheter the [catheter] snapped and remained inside the patient; a sizable chunk of the catheter (approximately 10 cm) remained inside the patient.There was no reported injury.Additional information received 14-jul-2022 reported, the product was in place for four (4) days, no injury was reported.The reporter noted that it was unclear if the patient would require surgery to remove the catheter.Additional information received 18-jul-2022 reported, the patient was due to have an x-ray once stable, in order to visualize the missing catheter, which was radio opaque.
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Manufacturer Narrative
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The product involved in the report has been returned and is being processed for evaluation.A review of the device history record is not possible as no lot number was provided.All information reasonably known as of 02 aug 2022 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 event reported but is relaying the information that was 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 21 cfr 803, 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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Manufacturer Narrative
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The actual sample from the reported event was returned for evaluation.A dual extension set of catheters was received: one of the catheters appeared intact, the second catheter was severed approximately 0.25inch below the single hash mark, the end did not appear stretched and was observed generally smooth.The reported event could be confirmed as reported; the root cause is undetermined.All information reasonably known as of (b)(6) 2022 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 event reported but is relaying the information that was provided by the user facility where the incident occurred.This product incident is documented in the avanos medical complaint database and identified as complaint comp-(b)(4).This information is submitted pursuant to (b)(4), 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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Search Alerts/Recalls
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