Catalog Number 0600041 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Peritonitis (2252)
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Event Type
Injury
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Manufacturer Narrative
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(b)(6).Should additional relevant information become available, a supplemental report will be submitted.
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Event Description
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It was reported that a patient underwent a lysis of adhesions procedure in which adept adhesion reduction solution and two other non-baxter products were used.It was reported that after use of the product, the patient experienced chemical peritonitis.It was reported a revision surgery was performed to assess the cause of abdominal pain the patient was experiencing.At the time of this report the patient¿s outcome was reported as ¿fine¿.No additional information is available.
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Manufacturer Narrative
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Additional information: should additional relevant information become available, a supplemental report will be submitted.
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Manufacturer Narrative
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Additional information: the device was not returned, and the lot number is unknown; therefore, a device analysis could not be completed.Should additional relevant information become available, a supplemental report will be submitted.
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Search Alerts/Recalls
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