Class II · Moderate risk
0.9% Sodium Chloride Injection
Lack of Assurance of Sterility
National Drug Code
Is NDC 65282-1510-01 recalled?
Sodium Chloride · 5 TRAY in 1 CARTON (65282-1510-1) / 5 AMPULE in 1 TRAY / 10 mL in 1 AMPULE
Yes — this exact package was recalled
1 FDA recall names the code 65282-1510-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Sodium Chloride
- Strength
- SODIUM CHLORIDE 9 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous, Subcutaneous
- Labeler
- Spectra Medical Deviecs, LLC
- Type
- Human Prescription Drug
- Product code
- 65282-1510
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
- 65282-1605 Lidocaine Hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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