---
title: "Medline RR-LIVER TRNS ACCESSORY PEDS, DUNJ63397; medical procedure convenienc... — FDA record Z-1173-2025 | Is It on Recall"
description: "Medline is recalling medical convenience kits which were assembled with specific Coloplast Foley catheters and Prostatic catheters which were subsequently recal"
url: https://isitonrecall.com/recall/fda-device-z-1173-2025-medline-rr-liver-trns-accessory-peds-dunj63397-medical-procedure-convenience-kit/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Medline RR-LIVER TRNS ACCESSORY PEDS, DUNJ63397; medical procedure convenience kit — FDA record Z-1173-2025

Reported ongoing

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 3, 2025. 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**: Medline RR-LIVER TRNS ACCESSORY PEDS, DUNJ63397; medical procedure convenience kit
- **Reason**: Medline is recalling medical convenience kits which were assembled with specific Coloplast Foley catheters and Prostatic catheters which were subsequently recalled due to a potential sterility issue detected during testing.
- **Classification**: Class II
- **Recalling firm**: MEDLINE INDUSTRIES, LP - Northfield
- **Quantity**: 36 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1173-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1173-2025%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 | UDI/DI 10193489736755 (ea) 40193489736756 (cs), Lot Numbers: 22HLA247, 21HLA443, 21JLA520, 22GLA335. |

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

## Distribution

US: CA

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

- [California](https://isitonrecall.com/state/california/)

## Dates in the source

- **Report date**: Feb 26, 2025
- **Recall initiation date**: Jan 3, 2025
- **Center classification date**: Feb 14, 2025

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-1173-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MEDLINE INDUSTRIES, LP - Northfield records](https://isitonrecall.com/brand/medline-industries-lp-northfield/)