---
title: "BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS16C — FDA record Z-0667-2022 | Is It on Recall"
description: "There is a potential to leak from the catheter where it connects to the drain bag"
url: https://isitonrecall.com/recall/fda-device-z-0667-2022-bard-surestep-intermittent-catheter-tray-14fr-ref-ints16c/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS16C — FDA record Z-0667-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 27, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS16C
- **Reason**: There is a potential to leak from the catheter where it connects to the drain bag
- **Classification**: Class II
- **Recalling firm**: C.R. Bard Inc
- **Quantity**: 1620 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0667-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0667-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Serial Number/UDI NGEWX117 (01)00801741183249(17) NGEXX133/(01)00801741183249(17) NGEY0842/(01)00801741183249(17) NGEZ1823/(01)00801741183249(17) |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Nationwide distribution in the states of GA, ME, NJ, WI, MN, SD, CO, ND, ID, IL, FL, LA, MD, PA, OH, NE.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Mar 2, 2022
- **Recall initiation date**: Jan 27, 2022
- **Center classification date**: Feb 24, 2022
- **Termination date**: Jul 10, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0667-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [C.R. Bard Inc records](https://isitonrecall.com/brand/c-r-bard-inc/)