Bard® Large Nylon Catheter Plug 0414LRecalls & reported problems

C. R. Bard, Inc. · Bard® Large Nylon Catheter Plug · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 1
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801741046244), received between Oct 17, 2025 and Oct 17, 2025 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Adverse Event Without Identified Device or Use Problem1

Patient problems

Unspecified Infection1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

InjuryOct 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT HAD A FOLEY, DRAIN BAG AND FOLEY PLUG. PATIENT HAS BEEN GETTING INFECTIONS CONSTANTLY AND WOULD LIKE TO KNOW HOW TO CLEAN THE FOLEY PLUG BETTER. UPON TROUBLESHOOTING, IT WAS NOTED THAT THE PATIENT WAS USING RUSCH FOLEY, CARDINAL DRAINAGE BAG AND BD FOLEY PLUG, 0414L. EXPLAINED WE HAVE NO CLEANING INFORMATION FOR THIS PLUG AND IT WAS NON-STERILE. SUGGESTED A STERILE FOLEY PLUG FROM MEDLINE AND REACH OUT TO HER HCP. CALLER WAS UNHAPPY WITH THIS INFORMATION AND HUNG UP. FORWARDED INFORMATION TO COMPLAINTS. IT IS UNKNOWN WHAT MEDICAL INFORMATION WAS PROVIDED.
Patient problems: Unspecified Infection
MAUDE report 23330333 ↗

Device details

UDI-DI	`10801741046244`
Brand	Bard® Large Nylon Catheter Plug
Model	0414L
Company	C. R. Bard, Inc.
Product code	KNY · ACCESSORIES, CATHETER, G-U
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	OTC
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Dec 4, 2020

Device type (GMDN): Urethral catheterization support kit, urinary drainage

A collection of non-surgically invasive devices intended to assist a healthcare professional to insert a urethral catheter (not included) into the urinary bladder, typically for drainage of urine; some types may also be intended for catheter removal. It typically includes forceps, dressings, gloves, and drapes; it does not include pharmaceuticals. This is a single-use device.

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Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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