# FDA recall Z-0509-2025

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

## Product

MEDLINE procedure kits labeled as follows:    1) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268B;   2) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268C;   3) FEMORAL BLOCK TRAY, REF DYNJRA1739A;   4) FEMORAL BLOCK TRAY, REF DYNJRA1739B;   5) 18G CPNB 20G STYLETED CATHETER, REF DYNJRA1869;   6) CONT EPID 18G NDL/20G CATH, REF DYNJRA9035;   7) TRAY 18G CPNB 20G STYLETED, REF DYNJRA9040;   8) CATHETER REINF W/ CONNECT OT, REF EPIREINF19O;   9) CATHETER REINF WITH CONNECTOR, REF EPIREINF29C;   10) CONTINUOUS EPIDURAL UPDATED, REF PAIN0384B;   11) CONT EPI 20G W/HUSTEAD, REF PAIN1069C;   12) CONTINUOUS EPIDURAL, REF PAIN1271A;   13) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN1281B;   14) CONTINUOUS EPIDURAL TRAY, REF PAIN1317;   15) 20G CONT. EPID TRAY, REF PAIN1353B;   16) CONTINUOUS EPIDURAL TRAY, REF PAIN1358;   17) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN1361;   18) JHAC CONT EPIDURAL, REF PAIN1437A;   19) CONTINUOUS EPIDURAL TRAY, REF PAIN1453B;   20) EPIDURAL CATH KIT, REF PAIN1536A;   21) CO

## 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-0509-2025
- **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-0509-2025

## Citation

> AI Analytics. FDA recall Z-0509-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0509-2025. Source: US FDA. Licensed CC0.

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