Catalog Number 9-PFO-2518 |
Device Problem
Air/Gas in Device (4062)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/08/2024 |
Event Type
malfunction
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Manufacturer Narrative
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Investigation is not yet complete.A follow-up report will be submitted with all additional relevant information.
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Event Description
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It was reported that on (b)(6) 2024, a 18-25mm amplatzer talisman patent foramen ovale (pfo) occluder (lot: 8864459) was chosen for implantation utilizing an 8f amplatzer talisman delivery sheath.During preparation, when attempting to advance the occluder into the delivery sheath, air bubbles appeared in the loader.Only when all connections, from the sheath to the loader, from the loader to the hemostasis valve and the hemostasis valve were submerged in a water bath, could the device be advanced without bubbles.The device was implanted successfully.No air entered the anatomy and no additional aspiration was needed to prevent air from entered the patient.There were no reported patient consequences or clinically significant delay.The patient remained hemodynamically stable throughout the procedure.
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Manufacturer Narrative
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An event of air while loading the occluder into the delivery sheath was reported.A returned device inspection, to rule out any device-related causes, could not be performed as the device was not returned for analysis.The device history record was reviewed to ensure that each manufacturing and inspection operation was performed, and the product met all specifications.Based on the information received, the cause of the reported incident could not be conclusively determined.There is no indication of a product quality issue with respect to labeling design or manufacturing of the device.
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Event Description
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It was reported that on (b)(6) 2024, a 18-25mm amplatzer talisman patent foramen ovale (pfo) occluder (lot: 8864459) was chosen for implantation utilizing an 8f amplatzer talisman delivery sheath.During preparation, when attempting to advance the occluder into the delivery sheath, air bubbles appeared in the loader.Only when all connections, from the sheath to the loader, from the loader to the hemostasis valve and the hemostasis valve were submerged in a water bath, could the device be advanced without bubbles.The device was implanted successfully.No air entered the anatomy and no additional aspiration was needed to prevent air from entered the patient.There were no reported patient consequences or clinically significant delay.The patient remained hemodynamically stable throughout the procedure.
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Search Alerts/Recalls
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