# FDA recall Z-1291-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2024-02-08.

## Product

CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401

## Reason for recall

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Clearlink Non-DEHP solution set listed below due to potential leaks originating from the drip chamber.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1291-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-08
- **Report date:** 2024-03-20

- **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-1291-2024

## Citation

> AI Analytics. FDA recall Z-1291-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1291-2024. Source: US FDA. Licensed CC0.

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