Baxter Solution Set with Duo-Vent Spike recall
Baxter Solution Set with Duo-Vent Spike, REF 2R8404
Why was Baxter Solution Set with Duo-Vent Spike recalled?
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 00085412676630, Lot Numbers: DR24C22079 (exp.3/247/2026), DR24H23086 (exp. 8/26/2026)
- Product
- Baxter Solution Set with Duo-Vent Spike, REF 2R8404
- Recalling firm
- Baxter Healthcare Corporation
- Distribution
- US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.
- Recall date
- January 29, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)