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

Is NDC 0990-7984-23 recalled?

Sodium Chloride · 48 POUCH in 1 CASE (0990-7984-23) / 1 BAG in 1 POUCH / 100 mL in 1 BAG

Recall announced for this product announced by the firm and posted by FDA; not yet in FDA’s classified recall data

Yes — this exact package was recalled

1 FDA recall names the code 0990-7984-23 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.

3 of these recalls are still ongoing.

Active ingredient
Sodium Chloride
Strength
SODIUM CHLORIDE 900 mg/100mL
Form
Injection, Solution · Intravenous
Labeler
ICU Medical Inc.
Type
Human Prescription Drug
Product code
0990-7984

Recalls naming this package

Unclassified

0.9% Sodium Chloride Injection

Product Mix-up: 0.9% SODIUM CHLORIDE Injection, USP may potentially contain the overwrap with labeling indicating it to be 0.9% SODIUM CHLORIDE Injection, USP but the actual product within the overwrap may be POTASSIUM CHLORIDE Inj.10 mEq

Ongoing Labeling / mix-up Otsuka ICU Medical LLC NDC 0990-7984-23 Recall number pending

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