Catalog Number 03P84-25 |
Device Problem
Incorrect, Inadequate or Imprecise Result or Readings (1535)
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Patient Problem
Pain (1994)
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Event Date 01/29/2021 |
Event Type
malfunction
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Manufacturer Narrative
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Apoc incident# (b)(4).Apoc labeling will be evaluated during the investigation as pertaining to the event.
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Event Description
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On 01-feb-2021, abbott point of care was contacted by a customer regarding i-stat crea cartridges that yielded a suspected discrepant creatinine result of 2.8 mg/dl on a (b)(6) year old female patient presented with pain, post-op hysterectomy.There was no patient information available at the time of this report.Return product is not available for investigation.Method:i-stat.Date: (b)(6) 2021.Collected: 1530.Tested: 153.Result: 2.8 mg/dl.Sample:venous.Method : (b)(6).Date : (b)(6) 2021.Collected : ni.Tested :ni.Result : 1.2 mg/dl.Sample: ni.There are no injuries associated with this event.At this time there is no reason to suspect a malfunction exists.The reporting decision was based on limited information available that suggests the product was not performing within the variability of the assay.The investigation is underway.
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Event Description
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Na.
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Manufacturer Narrative
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Apoc incident: (b)(4).The investigation was completed on (b)(6) 2021.A review of the device history record confirmed the lot passed finished goods release criteria.Retained cartridge testing met the acceptance criteria found in q04.01.003 rev.Af, appendix 1- product complaint level 2 and level 3 investigation procedure.No deficiency has been identified for crea cartridge lot a20278.
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