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

Is NDC 0409-6727-23 recalled?

Magnesium Sulfate in Dextrose · 24 POUCH in 1 CASE (0409-6727-23) / 1 BAG in 1 POUCH / 100 mL in 1 BAG (0409-6727-11)

Yes — this exact package was recalled

1 FDA recall names the code 0409-6727-23 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
Magnesium Sulfate in Dextrose
Strength
MAGNESIUM SULFATE HEPTAHYDRATE 10 mg/mL
Form
Injection, Solution · Intravenous
Labeler
Hospira, Inc.
Type
Human Prescription Drug
Product code
0409-6727

Recalls naming this package

Class I · High risk

Magnesium Sulfate in 5% Dextrose Injection

Labeling: Wrong Bar Code: There is a potential for some units to be mislabeled with an incorrect barcode on the immediate container that scans as heparin sodium 2000 USP units/1000 mL in 0.9% in sodium chloride injection.

Terminated Labeling / mix-up Hospira Inc. NDC 0409-6727-23 D-1076-2015

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