Catalog Number UNKNOWN |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Reaction (2414)
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Event Date 10/23/2020 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4) initial emdr submission.A follow up emdr will be submitted if additional information becomes available.(b)(4).
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Event Description
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Material no.: unknown ; batch no.: unknown.It was reported the patient experienced anaphylaxis while using chloraprep.Per letter: drug allergy: chloraprep one step: anaphylaxis.
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Event Description
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Material no.: unknown batch no.: unknown.It was reported the patient experienced anaphylaxis while using chloraprep.Per letter: drug allergy: chloraprep one step: anaphylaxis.
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Manufacturer Narrative
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No additional information was provided by physicians clinic of iowa.Primevigilance did reach out to obtain with no success.Should additional information be available in the future, the complaint will be re-opened and investigated.All complaints are reviewed during monthly quality/safety meetings.In addition, complaints are trended at monthly quality data analyst meetings and quarterly plant management review meetings h3 other text : see narrative below.
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Search Alerts/Recalls
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