Model Number N/A |
Device Problems
Defective Component (2292); Material Deformation (2976)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/08/2024 |
Event Type
malfunction
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Event Description
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Hold for rw 1.30 it was reported by customer that port-a-cath needle have been opened and found to be faulty.Needle was loose and white padding was halfway peeled off straight out of the package.No other information was provided.
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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 date of event was not provided by the complainant reporter, the date reflected in this report is the date bd became aware of the event.The device has not been returned to the manufacturer for evaluation.H3 other text : device not received.
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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.
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Event Description
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It was reported by customer that port-a-cath needle have been opened and found to be faulty.Needle was loose and white padding was halfway peeled off straight out of the package.No other information was provided.
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Search Alerts/Recalls
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