Class II · Moderate risk
8.4% Sodium Bicarbonate Injection
Lack of Assurance of Sterility
National Drug Code
Is NDC 51754-5001-05 recalled?
Sodium Bicarbonate · 20 VIAL in 1 CARTON (51754-5001-5) / 50 mL in 1 VIAL
Yes — this exact package was recalled
3 FDA recalls name the code 51754-5001-05 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.
2 of these recalls are still ongoing.
- Active ingredient
- Sodium Bicarbonate
- Strength
- SODIUM BICARBONATE 84 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Exela Pharma Sciences, LLC
- Type
- Human Prescription Drug
- Product code
- 51754-5001
Recalls naming this package
Class I · High risk
8.4% Sodium Bicarbonate Injection
Presence of Particulate Matter: Silicone
Class I · High risk
8.4% Sodium Bicarbonate Injection
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration.
Class I · High risk
8.4% Sodium Bicarbonate Injection
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Class II · Moderate risk
8.4% Sodium Bicarbonate Injection
Lack of Assurance of Sterility
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
- 51754-1007 Elcys 1
- 51754-2001 See recall 1
- 51754-2131 See recall 1
- 51754-5012 Sodium Bicarbonate 1
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