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Model Number N/A |
Device Problem
Activation Problem (4042)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 08/24/2020 |
Event Type
malfunction
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Manufacturer Narrative
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The device has not been returned to the manufacturer for evaluation.A lot history review (lhr) review is not possible, as no manufacturing lot number has been provided by the complainant.
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Event Description
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It was reported that during removal, the safety mechanism could not be activated.
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Manufacturer Narrative
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H11:section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.The initial complaint appeared to be a reportable occurrence.Once the sample was returned and evaluated it was determined that a reportable event had not occurred.
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Event Description
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It was reported that during removal, the safety mechanism could not be activated.
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Search Alerts/Recalls
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