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Model Number 21-7302-24 |
Device Problems
Device Alarm System (1012); Failure to Sense (1559)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/13/2021 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(6).
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Event Description
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Information was received indicating that while in use of a smiths medical cadd cassette reservoir, it was noted that the cassette could not be recognized by the pump.No patient consequences were reported.No adverse effects were reported.
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Manufacturer Narrative
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No product or photographic evidence were provided to aid in this investigation.The complaint report offered insufficient details to determine whether this product functioned as intended or was used in a manner consistent with its instructions for use (ifu) or failed to meet product specifications.Lacking any additional evidence, this complaint has been closed as unconfirmed.If the product is returned, smiths medical will reopen this complaint for further investigation.
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Search Alerts/Recalls
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