---
title: "MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001 — FDA record Z-0202-2023 | Is It on Recall"
description: "Some of the labels of the kits for product code 10-4001 in the specified lots have an illegible barcode which prevents successful scanning of the package."
url: https://isitonrecall.com/recall/fda-device-z-0202-2023-med-rx-urological-cysto-bladder-irrigation-set-ref-10-4001/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001 — FDA record Z-0202-2023

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 Aug 19, 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**: MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001
- **Reason**: Some of the labels of the kits for product code 10-4001 in the specified lots have an illegible barcode which prevents successful scanning of the package.
- **Classification**: Class III
- **Recalling firm**: Canadian Hospital Specialties
- **Quantity**: 9100 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0202-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0202-2023%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: 00628725001050, Lot Numbers: 159603, exp 2026-12-01 and 166945, exp 2027-06-01 |

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

## Distribution

US

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Nov 23, 2022
- **Recall initiation date**: Aug 19, 2022
- **Center classification date**: Nov 11, 2022
- **Termination date**: Mar 20, 2023

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-0202-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Canadian Hospital Specialties records](https://isitonrecall.com/brand/canadian-hospital-specialties/)