Catalog Number H938724 |
Device Problem
Free or Unrestricted Flow (2945)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
malfunction
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Manufacturer Narrative
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Manufacturing facility-this device was manufactured at one of the two following manufacturing sites: (b)(4) baxter healthcare.Should additional relevant information become available, a supplemental report will be submitted.
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Event Description
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It was reported cloudy bags were observed during compounding with the em2400 valve set.Lipids were used at port 5 and the cloudy bags were non-tpn.There was no patient involvement.No additional information is available.
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Manufacturer Narrative
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H10: the device was not returned and the lot number is unknown; therefore, a device analysis could not be completed.Should additional relevant information become available, a supplemental report will be submitted.
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Search Alerts/Recalls
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