Model Number N/A |
Device Problem
Material Twisted/Bent (2981)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 03/24/2022 |
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 the io needle was bent.It was reported "during a cardiac arrest on b shift today two yellow 45 mm i o needles bent during non-forceful insertion.The primary site of the humeral head bent as well as secondary site of the tibia.The emt attempted both sites stated they were not inserted under excess pressure." this report addresses the first device used in the humeral head.
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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.
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Event Description
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It was reported the io needle was bent.It was reported "during a cardiac arrest on b shift today two yellow 45 mm i o needles bent during non-forceful insertion.The primary site of the humeral head bent as well as secondary site of the tibia.The emt attempted both sites stated they were not inserted under excess pressure." this report addresses the first device used in the humeral head.
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Search Alerts/Recalls
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