FDAFDA · Food and drugs·Recall number Z-1291-2024
CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401
Published March 20, 2024 · Recall initiated: February 8, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- US Nationwide distribution.
- Lot
- UDI/DI 00085412565767, Lot Number R23A02062, exp. 1 Jan 2025
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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