# FDA recall Z-0513-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-10-16.

## Product

MEDLINE procedure kits labeled as follows:   1)	CONT EPI 20G W/HUSTEAD,	REF PAIN1069B;  2)	CSE TRAY,	REF PAIN1941;  3)	TRAY CON EPID 20G NYL W/TUOHY, REF PAIN9023;  4)	TRAY, CONT EPI 20G NYL W/ HUST,	REF PAIN1281  5)   TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN9024

## Reason for recall

The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

## Distribution

US Nationwide.  Bermuda, Canada, Panama, UAE, US Virgin Islands

## Key facts

- **Recall number:** Z-0513-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-16
- **Report date:** 2024-12-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0513-2025

## Citation

> AI Analytics. FDA recall Z-0513-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0513-2025. Source: US FDA. Licensed CC0.

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