Reported Apr 15, 2026 · Ongoing
0.9% Sodium Chloride Injection, USP, (2,250 mg per 250 mL) (9 mg per mL) 250 mL in a 250 mL freeflex bag, Rx only,…
Fresenius Kabi USA, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Fresenius Kabi USA, LLC · 3 Corporate Dr · Lake Zurich, IL · 60047-8930
Is this the product you have?
- 0.9% Sodium Chloride Injection, USP, (2,250 mg per 250 mL) (9 mg per mL) 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047
- Unit of Use NDC65219-470-05
- Unit of Sale NDC Number65219-470-30
- Lot codes and dates
7 of 7 products
Products covered by this recall # Product as published 1 12/31/2026 2 Batch# 24JU10003, Exp Date: 07/31/2027 3 Batch# 24LU10011, 24LU10012, Exp Date: 9/30/2027 4 Batch# 6402273, 6402275, Exp Date: 01/31/2028 5 Batch# 6402420, 6402421, 6402422, 6402423, Exp Date: 03/31/2028 6 Batch# 6402473, 6402474, 6402475, 6402476, 6402485, Exp Date: 04/30/2028 7 Batch# 6402516, Exp Date: 05/31/2028.
This recall covers 14 products
The agency filed one notice per product. You are reading one of them; the other 13 are below.
1 more are in the archive.
Where it was sold
Why it was recalled
Lack of Assurance of Sterility
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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