MAUDE Adverse Event Report: C.R. BARD, INC. (BASD) -3006260740 POWERPORT IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F; PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

Catalog Number 1708000

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Thrombosis/Thrombus (4440)

Event Date 03/26/2024

Event Type  Injury  

Manufacturer Narrative

H10: manufacturing review: a manufacturing review was not requested as the lot number reported as unknown.Investigation summary: the physical device was not returned for evaluation.No medical record were provided for review.Therefore, the investigation is inconclusive for the reported failure as no objective evidence was provided for review.Based upon the available information, the definitive root cause is unknown.Labeling review: as the reported event did not allege a labeling or use related issue, a labeling review is not required.H11: section a through f ¿ 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.

Event Description

It was reported through the litigation process that sometime post a port placement, the patient allegedly developed thrombosis.However, the current status of the patient is unknown.

Event Description

It was reported through the litigation process that sometime post a port placement via the right subclavian vein, the patient allegedly developed with thrombosis.Reportedly, the port and catheter were removed intact and replaced with a new port.The current status of the patient is unknown.

Manufacturer Narrative

Manufacturing review: a manufacturing review was not requested as the lot number reported as unknown.Investigation summary: the physical device was not returned for evaluation.Medical records were provided and reviewed.The medical record alleges infuse the port placement to the right subclavian vein for the patient with the crohn's disease and need for long term iv access.The board placement was take place by made a blunt finger dissection and the catheter was cut and assembled yeah delete sheet was threaded over the wire and through the catheter and through the sheet with the help of fluoroscopic guidance and the tip of the catheter at the right atrium.The catheter was aspirated and flushed without any difficulty and happiness with saline.The port was then suited to scrappers fascia.On an unknown date it was planned to remove the port as there was a possible of nidus of clot formation.Approximately a month later of post placement of port yeah dermatotomy was made at the site of the healed incision, using both blend and sharp dissection the port and catheter were freed from the surrounding of their soft tissue and further the incision was closed.Approximately a month later an 8 french power port was placed with the help of ultrasound and fluoroscopic guidance at the left internal jugular vein and attention was turned for the creation of the subcutaneous packet and tunnel.Then your packet was made with the blunt dissection yeah tunneling tool was passed and catheter was pulled through the initial venotomy site.Then the catheter was cut to the length and attach it to the port reservoir.The introducer of the coaxial catheter was removed and the guidewire was passed into the inferior vena cava yeah micro puncture sheet was a change for appeal away and the catheter was advanced through the sheet and positioned centrally using the fluoroscopy.The patient tolerates the procedural well.Therefore, the investigation is inconclusive as no objective evidence for the reported deficiency with the port in the submitted medical record review.Additionally, it can be confirmed that the patient experienced thrombosis.However, the relationship to the port is unknown.Furthermore, the clinical condition alleged in the complaint cannot be confirmed.Based upon the available information, the definitive root cause is unknown.Labeling review: as the reported event did not allege a labeling or use related issue, a labeling review is not required.` section a through f ¿ 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.

• Brand Name: POWERPORT IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F
• Type of Device: PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR
• Manufacturer (Section D): C.R. BARD, INC. (BASD) -3006260740; 605 north 5600 west; salt lake city 84116
• Manufacturer (Section G): BARD REYNOSA S.A. DE C.V. -9617592; blvd. montebello #1; parque industrial colonial; reynosa, tamaulipas 88780 ; MX 88780
• Manufacturer Contact: brett curtice ; 800 w. rio salado pkwy; tempe, AZ 85281 ; 4803032689
• MDR Report Key: 19046973
• MDR Text Key: 339547617
• Report Number: 3006260740-2024-01466
• Device Sequence Number: 1
• Product Code: LJT
• UDI-Device Identifier: 00801741026577
• UDI-Public: (01)00801741026577
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K060812
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Health Professional
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date: 04/25/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 1708000
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 03/26/2024
• Initial Date FDA Received: 04/04/2024
• Supplement Dates Manufacturer Received: 05/03/2024
• Supplement Dates FDA Received: 05/09/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 49 YR
• Patient Sex: Male