Class II · Moderate risk
Sodium Chloride Injection
Presence of Particulate Matter: Confirmed customer report of visible particulate in the form of an orange or rust colored ring embedded in between the plastic layers of the plastic vial.
National Drug Code
Is NDC 0409-4888-20 recalled?
Sodium Chloride · 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-20) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-4888-03)
Yes — this exact package was recalled
1 FDA recall names the code 0409-4888-20 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Sodium Chloride
- Strength
- SODIUM CHLORIDE 9 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous, Subcutaneous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-4888
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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