Model Number 2420-0007 |
Device Problem
Fluid/Blood Leak (1250)
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Patient Problems
Venipuncture (2129); No Consequences Or Impact To Patient (2199)
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Event Date 05/06/2019 |
Event Type
malfunction
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Manufacturer Narrative
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The devices have been received and the evaluation is pending.A follow up report will be submitted with investigation results once the evaluation has been completed.
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Event Description
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The reported feedback suggests that there are connection issues.From the reported information there are no indications of serious injury to the patient or user as a result of this incident.
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Manufacturer Narrative
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The customer's report of connection issues was confirmed.A visual inspection confirmed the customer's report as the sample was received without a male luer.A closer inspection did not identify any solvent around the end of the tubing.The root cause of the customer's report was due to an insufficient amount of solvent having been applied to the tubing during the assembly process.
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Event Description
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The reported feedback suggests that there are connection issues.
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Search Alerts/Recalls
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