Class II · Moderate risk
Potassium Chloride for Injection Concentrate USP
Lack of assurance of sterility: pinholes, within the blue label characters on the EXCEL bag, specifically within the dotted characters on the label, resulting in leaks.
National Drug Code
Is NDC 0264-1944-20 recalled?
Potassium Chloride · 24 CONTAINER in 1 CASE (0264-1944-20) / 250 mL in 1 CONTAINER
Yes — this exact package was recalled
1 FDA recall names the code 0264-1944-20 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
- Potassium Chloride
- Strength
- POTASSIUM CHLORIDE 14.9 g/100mL
- Form
- Injection, Solution, Concentrate · Parenteral
- Labeler
- B. Braun Medical Inc.
- Type
- Human Prescription Drug
- Product code
- 0264-1944
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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