Catalog Number 07K70-25 |
Device Problem
High Test Results (2457)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 07/27/2016 |
Event Type
malfunction
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Manufacturer Narrative
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Patient identifier did not contain enough spaces for entire patient id.The entire patient id is (b)(4).This report is being filed on an international product, list 7k70 that has a similar product distributed in the u.S., list 6c06.An evaluation is in process.A followup report will be submitted when the evaluation is complete.An evaluation in process.
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Event Description
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The account generated false elevated architect total psa of >100.00 ng/ml on id (b)(6) that did not match clinical diagnosis.Historically, the patient tested architect psa of 9.4 ng/ml on (b)(6) 2016 and had a negative needle biopsy and psa of 14.9 ng/ml in (b)(6) 2015.No impact to patient management was reported.
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Manufacturer Narrative
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The ticket searches determined that there is no unusual activity for the likely cause lot for this issue and the complaint trending report review determined that there is no non statistical or adverse trend for the issue for the product.No patient sample was available for evaluation.Therefore, testing of a serum based panel sample which mimics a patient sample was performed.All specifications were met indicating the complaint lot is performing acceptably.A review of the manufacturing documentation did not identify any issues associated with the customer observation.A review of the product labeling concluded that the issue is sufficiently addressed.Based on all available information and evaluation, the assay performed as intended and no product deficiency was identified.
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Manufacturer Narrative
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The device evaluation was reassessed and concluded that a malfunction occurred, therefore, the device was not performing as intended at the customer site.However, no systemic issue and/or product deficiency was identified.The conclusion code in evaluation codes was changed from (b)(4).
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Search Alerts/Recalls
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