Reported Apr 15, 2026 · Ongoing
0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 100 mL in a Single Dose freeflex bag, Rx only, BD…
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, 900 mg per 100 mL (9 mg per mL) 100 mL in a Single Dose freeflex bag, Rx only, BD Beckton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417 USA, Distributed by BD
- Manufactured byFresenius Kabi USA, LLC ("Fresenius Kabi")
- Unit of Sale NDC Number17271-701-03
- Lot codes and dates
7 of 7 products
Products covered by this recall # Product as published 1 11/30/2026 2 Batch# 6402297, 6402298, Exp Date: 01/31/2027 3 Batch# 6402377, 6402378, 6402379, Exp Date: 02/28/2027 4 Batch # 6402429, 6402430, 6402431, 6402432, 6402433, Exp Date: 03/31/2027 5 Batch# 6402434, Exp Date: 04/30/2027 6 Batch# 6402512, Exp Date: 05/2027 7 Batch# 6402574, 6402576, Exp Date: 06/30/2027.
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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