Class II · Moderate risk
DIANEAL Low Calcium
Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.
National Drug Code
Is NDC 0941-0409-07 recalled?
DIANEAL Low Calcium with Dextrose · 5000 mL in 1 BAG (0941-0409-07)
Yes — this exact package was recalled
3 FDA recalls name the code 0941-0409-07 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, sodium lactate, calcium chloride, magnesium chloride and dextrose
- Strength
- DEXTROSE MONOHYDRATE 1.5 g/100mL; SODIUM CHLORIDE 538…
- Form
- Injection, Solution · Intraperitoneal
- Labeler
- Vantive US Healthcare LLC
- Type
- Human Prescription Drug
- Product code
- 0941-0409
Recalls naming this package
Class II · Moderate risk
Dianeal Low Calcium
Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.
Class II · Moderate risk
DIANEAL Low Calcium
Defective Container: There is a potential for frangible components to be broken, resulting in a leak at the port when the closure is removed.
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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