C.R. BARD, INC. (BASD) -3006260740 POWERPORT TI L/P 6 CF INT WOSP ATT SL; PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR
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Catalog Number 8716001 |
Device Problems
Device Damaged Prior to Use (2284); Deformation Due to Compressive Stress (2889)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/23/2024 |
Event Type
malfunction
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Manufacturer Narrative
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H10: as the lot number for the device was provided, a review of the device history records is currently being performed.The device was not returned to the manufacturer for inspection/evaluation.However, a photo was provided for review.The investigation of the reported event is currently underway.H10: d4 (expiry date: 04/2025).H11: the information provided by bd represents all 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 that prior to a port placement procedure, the catheter was allegedly distorted in multiple places.The procedure was completed using another device.There was no patient contact.
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Search Alerts/Recalls
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