Catalog Number 688957 |
Device Problems
Fracture (1260); Material Separation (1562)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 04/02/2020 |
Event Type
malfunction
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Manufacturer Narrative
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The suspect device has been returned for evaluation.A follow up will be submitted when the evaluation is complete.
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Event Description
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The account alleges that a connector detached from the infustion set.No patient injury to report.
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Manufacturer Narrative
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The suspect device was returned for evaluation.Visual examination was performed.The complaint was confirmed.The root cause could not be determined.A review of the device history and complaint database could not be performed since the lot number was not provided.
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Search Alerts/Recalls
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