# FDA recall Z-0202-2023

> **Canadian Hospital Specialties** · Class III · device recall initiated 2022-08-19.

## Product

MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001

## Reason for recall

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.

## Distribution

US

## Key facts

- **Recall number:** Z-0202-2023
- **Recalling firm:** Canadian Hospital Specialties
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-08-19
- **Report date:** 2022-11-23
- **Termination date:** 2023-03-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oakville, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0202-2023

## Citation

> AI Analytics. FDA recall Z-0202-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0202-2023. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
