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Model Number N/A |
Device Problem
Defective Component (2292)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 09/10/2021 |
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) of refs0074 showed no other similar product complaint(s) from this lot number.
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Event Description
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It was reported customer opened a midline kit, and the one of the needles in the kit was loose (without a cover).No other information was provided.
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Search Alerts/Recalls
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