Model Number N/A |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Ulcer (2274)
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Event Date 09/22/2021 |
Event Type
Injury
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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 by the customer "patient bent arm while sleeping and caused a pressure injury to the inner arm, opposite side of midline.".
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Event Description
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It was reported by the customer "patient bent arm while sleeping and caused a pressure injury to the inner arm, opposite side of midline.".
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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.Initial medwatch report was submitted, upon further review it was found that this medwatch report 3006260740-2022-02768 is a duplicate file and has been voided.The original event was submitted on medwatch report 3006260740-2022-02768.
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Search Alerts/Recalls
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