Class II
FDA
Baxter Anticoagulant Sodium Citrate Solution recalled over Foreign material
Baxter Anticoagulant Sodium Citrate Solution was recalled on August 26, 2026 because of foreign material. It is a Class II recall (possible temporary or reversible harm). Affected area: nationwide. Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
HazardForeign material
Risk levelClass II
Affected areaNationwide
CategoryFood
What to do
Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Confirm the details against the official FDA notice before acting.
Does this affect you?
Check the product in your home against the recalled item:
- Product as filed
- Baxter — Voluntary Nationwide Recall for One Lot of Anticoagulant Sodium Citrate Solution Due to Potential Presence of Particulate Matter
The notice lists no UPC or lot code. Match the brand, product name and package size against the official FDA notice.
Full recall details
- Reason for recall
- FOR IMMEDIATE RELEASE – AUG. 25, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling one lot of Anticoagulant Sodium Citrate Solution due to the potential presence of particulate matter identified as fiberglass in the solution.
- Hazard class
- Class II — possible temporary or reversible harm
- Recalling company
- Baxter
- Recall type
- Voluntary
- Quantity
- Distribution
- The impacted product was distributed from 7/2/2026 to 7/11/2026 to one customer in the United States.
Compiled from the official FDA record by our data rules — how we build these pages. Spotted an error? Report it.
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