# FDA recall Z-2594-2025

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2025-08-08.

## Product

Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519;  intravascular administration set

## Reason for recall

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2594-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-08
- **Report date:** 2025-10-01

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2594-2025

## Citation

> AI Analytics. FDA recall Z-2594-2025. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-2594-2025. Source: US FDA. Licensed CC0.

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