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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