Catalog Number 831165 |
Device Problems
Use of Device Problem (1670); Dull, Blunt (2407); Manufacturing, Packaging or Shipping Problem (2975)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 10/02/2023 |
Event Type
malfunction
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Event Description
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End user reports bending syringe cannulas during injection.Syringes are being pre-filled and stored in fridge before use.
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Manufacturer Narrative
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Initial trend analysis for lot 58175 was conducted, no malfunctions were found.This is the only complaint for lot 58175.Further investigation will be conducted to determine the root cause of complaint.
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Event Description
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End user reports bending syringe cannulas during injection.Syringes are being pre-filled and stored in fridge before use.
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Manufacturer Narrative
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Retained lot samples for syringe lot 58175 were tested for needle sharpness, no abnormalities were found during testing.
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Search Alerts/Recalls
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