FDAFDA · Food and drugs·Recall number D-0169-2021
Sodium Chloride Injection, USP, 0.9%, 0.308 mOsmol/ml, 2mL Single Dose Vial, Rx Only, Mfd. by. West-ward Eatontown, NJ 07724 USA, Vial NDC 0641-0497-17
Published December 23, 2020 · Recall initiated: December 7, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed pH Specifications: Out of Specification pH Test Results were found in Sodium Chloride Injection USP 0.9% 2ml vial.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- SODIUM CHLORIDE
- Manufacturer
- Hikma Pharmaceuticals USA Inc.
- Distributor
- Distributed Nationwide in the USA
- Lot
- Lot#: 048315 EXP 4/2021; 068320 EXP 6/2021; 128302 EXP 12/2021; 099349 EXP 9/2022.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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