MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 BARDEX® ALL-SILICONE FOLEY CATHETER; LATEX FOLEY CATHETER

Catalog Number 165816

Device Problems Fluid/Blood Leak (1250); Split (2537)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Type  Injury  

Manufacturer Narrative

The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.The information provided by bard 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 bard.The device was not returned.

Event Description

It was reported that the tubing on the catheter had split and caused urine leakage.It was later reported that the patient had a bladder tumor, and had a catheter placed with a leg bag, and night bag.The catheter was placed on the friday, after having a speciality catheter removed.The following day, the catheter had a split circumferentially, just above the bifurcation area.The patient had not used a securement device for keeping the catheter in place.When the patient went to the hospital, they removed the catheter.Also, the patient was checked to ensure he could pass urine on 3 separate occasions, which would enable him to leave the hospital.A bladder scan was conducted 5 days later to check that his bladder was emptying urine and worked sufficiently.No further treatment was required.

Manufacturer Narrative

The information provided by bard 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 bard.The device was not returned.

Event Description

It was reported that the tubing on the catheter had split and caused urine leakage.It was later reported that the patient had a bladder tumor, and had a catheter was placed with a leg bag and night bag.The catheter was placed on the friday after having a speciality catheter removed.The following day, the catheter had a split circumferentially, just above the bifurcation area.The patient had not used a securement device for keeping the catheter in place.When the patient went to the hospital, they removed the catheter.Also, the patient was checked to ensure he could pass urine on 3 separate occasions, which would enable him to leave the hospital.A bladder scan was conducted 5 days later to check that his bladder was emptying urine and worked sufficiently.No further treatment was required.

Manufacturer Narrative

The device was not returned for evaluation.The device history record was reviewed and found nothing that could have caused or contributed to the reported event.The instructions for use state the following: "warning: do not use ointments or lubricants having a petrolatum base.They will damage silicone.Visually inspect the product for any imperfections or surface deterioration prior to use.Use luer tip syringe to inflate.Or for pre-filled products, remove clip and squeeze reservoir to inflate with stated ml of sterile water.Storage: store catheters at room temperature away from direct exposure to light, preferably in the original box.For urological use only.Refer to direct unit label for product content and gender specific use where applicable.To deflate catheter balloon: gently insert a luer slip tip syringe in the catheter valve.Never use more force than is required to make the syringe ¿stick¿ in the valve.Allow the pressure within the balloon to force the plunger back and fill the syringe with water.If you notice slow or no deflation, re-seat the syringe gently.Use only gentle aspiration to encourage deflation if needed.Vigorous aspiration may collapse the inflation lumen, preventing balloon deflation.If necessary, contact adequately trained professional for assistance, as directed by hospital protocol.Should balloon rupture occur, care should be taken to assure that all balloon fragments have been removed from the patient.Should balloon rupture occur, care should be taken to assure that all balloon fragments have been removed from the patient.Refer to direct unit label for sterilization method utilized.Bard, bardex, bardia, biocath and lubricath are trademarks and/or registered trademarks of c.R.Bard, inc.Or an affiliate.Warning: after use, this product may be a potential biohazard.Handle and dispose of in accordance with accepted medical practice and applicable laws and regulations." 1354, 2199: "nl".

Event Description

It was reported that the tubing on the catheter had split and caused urine leakage.It was later reported that the patient had a bladder tumor, and had a catheter was placed with a leg bag and night bag.The catheter was placed on the friday after having a speciality catheter removed.The following day, the catheter had a split circumferentially, just above the bifurcation area.The patient had not used a securement device for keeping the catheter in place.When the patient went to the hospital, they removed the catheter.Also, the patient was checked to ensure he could pass urine on 3 separate occasions, which would enable him to leave the hospital.A bladder scan was conducted 5 days later to check that his bladder was emptying urine and worked sufficiently.No further treatment was required.

• Brand Name: BARDEX® ALL-SILICONE FOLEY CATHETER
• Type of Device: LATEX FOLEY CATHETER
• Manufacturer (Section D): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; lot 57c; covington GA 30014
• Manufacturer (Section G): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; lot 57c; covington GA 30014
• Manufacturer Contact: amy gravley ; 8195 industrial blvd; covington, GA 30014 ; 7707846100
• MDR Report Key: 6747946
• MDR Text Key: 81298835
• Report Number: 1018233-2017-04000
• Device Sequence Number: 1
• Product Code: EZL
• Combination Product (y/n): N
• Reporter Country Code: GB
• PMA/PMN Number: K040504
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: consumer,other
• Reporter Occupation: Patient
• Type of Report: Initial,Followup,Followup
• Report Date: 01/11/2018

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 Expiration Date: 05/01/2021
• Device Catalogue Number: 165816
• Device Lot Number: MYBPE016
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 07/04/2017
• Initial Date FDA Received: 07/27/2017
• Supplement Dates Manufacturer Received: 07/04/2017; 01/09/2018
• Supplement Dates FDA Received: 07/28/2017; 01/11/2018
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 02/14/2017
• 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): Other; Required Intervention