MAUDE Adverse Event Report: C.R. BARD, INC. (BASD) -3006260740 NAVARRE BILIARY DRAIN; CHRONIC CATHETERS

Catalog Number	NBD8
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/17/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
H11: as the lot number for the device was provided, a review of the device history records is currently being performed.The device has not been returned to the manufacturer for evaluation.However, photos were provided for review.The investigation of the reported event is currently underway.Section a through f ¿ the information provide 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 or Problem Description
On (b)(6) 2025, a patient underwent an ultrasound guided percutaneous drainage catheter placement procedure using navarre biliary drainage catheter.Post the procedure, the drainage catheter was allegedly fractured.The procedure was completed using another device.There was no reported patient injury.
Additional Manufacturer Narrative
H11: manufacturing review: the device history records have been reviewed, and this lot met all release criteria.Investigation summary: the physical device was not returned for evaluation, three photos were provided for review.The first photo shows a partial view of the drainage catheter held by a clinician.The stylet is noted to be partially advanced through the catheter.No anomalies can be noted on the hub area.The second photo shows a partial view of the drainage catheter along with metal and plastic stylets held by a clinician.The metal stylet is noted to be partially advanced through the catheter.No anomalies can be noted on the hub area.The third photo shows a partial view of the drainage catheter along with stylets kept in a product pouch held by a clinician.The stylet is noted to be partially advanced through the catheter.The investigation is inconclusive for the reported fracture issue as the provided photo was not sufficient to confirm the reported issues for all the three devices.The definitive root cause could not be determined based upon available information.Labelling review: as the reported event did not allege a labeling or use related issue, a labeling review is not required.B5, d4 (unique identifier (udi) #), g3, h6 (component, method, result, conclusion) section a through f ¿ the information provide 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 or Problem Description
On (b)(6) 2025, a patient underwent an ultrasound guided percutaneous drainage catheter placement procedure using navarre biliary drainage catheter.Post the procedure, the drainage catheter was allegedly fractured.The procedure was completed using another device.There was no reported patient injury.

• Brand Name: NAVARRE BILIARY DRAIN
• Common Device Name: CHRONIC CATHETERS
• Manufacturer (Section D): C.R. BARD, INC. (BASD) -3006260740; 605 north 5600 west; salt lake city 84116
• Manufacturer (Section G): C.R. BARD, INC. (GFO); 289 bay road; queensbury 12804
• Manufacturer Contact: brett curtice ; 800 w. rio salado pkwy; tempe, AZ 85281 ; 4803032689
• MDR Report Key: 23242443
• Report Number: 3006260740-2025-07538
• Device Sequence Number: 18746707
• Product Code: FGE
• UDI-Device Identifier: 00801741036866
• UDI-Public: (01)00801741036866(11)220719(17)250628(10)GFGT1028
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: K955110
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 02/12/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 06/28/2025
• Device Catalogue Number: NBD8
• Device Lot Number: GFGT1028
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/17/2025
• Supplement Date Received by Manufacturer: 02/12/2026
• Initial Report FDA Received Date: 10/08/2025
• Supplement Report FDA Received Date: 02/13/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 07/19/2022
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown