Catalog Number 990173 |
Device Problem
Loose or Intermittent Connection (1371)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 09/14/2018 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(6).A device evaluation and/or device history review is anticipated, but is not complete.Upon completion, a supplemental report will be filed.
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Event Description
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It was reported that bd plastipak¿ syringe plunger was loose.No serious injury or medical intervention was reported.
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Manufacturer Narrative
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Batch history (dhr) analysis, maintenance records and quality notifications were performed and no deviation was found for this lot.No photos/samples were taken by the client for evaluation, it was not possible to carry out an investigation and determine the root cause for the incident.The production processes are validated according to the defined acceptance criteria.In this way it is not possible to confirm the complaint.
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Event Description
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It was reported that bd plastipak syringe plunger was loose.No serious injury or medical intervention was reported.
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Search Alerts/Recalls
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