Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0941-0457-01 recalled?

DIANEAL Low Calcium with Dextrose · 6000 mL in 1 BAG (0941-0457-01)

Yes — this exact package was recalled

1 FDA recall names the code 0941-0457-01 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, sodium lactate, calcium chloride, magnesium chloride and dextrose
Strength
DEXTROSE MONOHYDRATE 2.5 g/100mL; SODIUM CHLORIDE 538…
Form
Injection, Solution · Intraperitoneal
Labeler
Vantive US Healthcare LLC
Type
Human Prescription Drug
Product code
0941-0457

Recalls naming this package

Class II · Moderate risk

Dianeal Low Calcium

Lack of Assurance of Sterility: Potential presence of leaks originating from the Connector Assembly component.

Ongoing Sterility / contamination Baxter Healthcare Corporation D-0587-2024
Class I · High risk

Dianeal Low Calcium

Presence of Particulate Matter: particulate matter was found during the manufacturing process.

Terminated Particulate / foreign matter Baxter Healthcare Corp. NDC 0941-0457-05 D-1610-2014

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