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Food & drug recall · FDAMarch 11, 2026Serious

Fresenius Kabi USA, LLC — 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 NDC: 65219-470-05, U

Do not stop taking this without speaking to your pharmacist or doctor.

What’s wrong

Lack of Assurance of Sterility

The Recall Registry rates this serious — FDA Class II: temporary or medically reversible health harm.

What to do

Check the lot numbers below against what you have. Do not stop taking a prescription medicine because of a recall without speaking to your pharmacist or doctor first — for many medicines stopping is more harmful than continuing, and they can tell you whether yours is affected and what to do about it.

Who to contact: Recalling firm: Fresenius Kabi USA, LLC

The product

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 NDC: 65219-470-05, Unit of Sale NDC Number: 65219-470-30.

Details

Recall date
March 11, 2026
Brand
Fresenius Kabi USA, LLC
Model, lot or SKU numbers
Batch# 23SU10008, Exp Date: 12/31/2026Batch# 24JU10003, Exp Date: 07/31/2027Batch# 24LU10011, 24LU10012, Exp Date: 9/30/2027Batch# 6402273, 6402275, Exp Date: 01/31/2028Batch# 6402420, 6402421, 6402422, 6402423, Exp Date: 03/31/2028Batch# 6402473, 6402474, 6402475, 6402476, 6402485, Exp Date: 04/30/2028Batch# 6402516, Exp Date: 05/31/2028.
Where it was distributed

US Nationwide , Alaska, and Puerto Rico

The official notice

This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.

Their exact wording: “Fresenius Kabi USA, LLC — 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 NDC: 65219-470-05, U”

Read it on FDA →

Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.

Filed under: Prescription medicine

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