C.R. BARD, INC. (BASD) -3006260740 POWERLOC SAFETY INFUSION SET 20G X 0.75IN; SET, ADMINISTRATION, INTRAVASCULAR
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Model Number N/A |
Device Problem
Tear, Rip or Hole in Device Packaging (2385)
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Patient Problem
Anxiety (2328)
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Event Date 04/17/2023 |
Event Type
malfunction
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Event Description
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It was reported, the indentation packaging was found to be damaged.When using the disposable implantable drug delivery device for the patient.And the indentation needle was replaced immediately.This incident caused some anxiety and unease to the patient.
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Manufacturer Narrative
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H11: section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.The device has not been returned to the manufacturer for evaluation.H3 other text: device not returned for evaluation.
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Search Alerts/Recalls
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