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FDAFDA · Food and drugs·Recall number D-0434-2026

0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL), 1,000 mL in a Single Dose freeflex bag, Rx only, BD Becton, Dickson and Company, 1 Becton Drive, Franklin Lakes, NJ 07417, Distributed by BD, Manufactured by Fresenius Kabi, Unit of Sale NDC Number: 17271-701-07.

Published April 15, 2026 · Recall initiated: March 11, 2026

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Lack of Assurance of Sterility

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
SODIUM CHLORIDE
Manufacturer
Fresenius Kabi USA, LLC
Distributor
US Nationwide , Alaska, and Puerto Rico.
Lot
Batch# 24EU10010, Exp Date: 05/31/2027.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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