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

Is NDC 32909-0814-53 recalled?

Tagitol V

Yes — this exact package was recalled

1 FDA recall names the code 32909-0814-53 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
Barium Sulfate
Strength
BARIUM SULFATE 400 mg/mL
Form
Suspension · Oral
Labeler
E-Z-EM Canada Inc
Type
Human Prescription Drug
Product code
32909-0814

Recalls naming this package

Class III ยท Low risk

Tagitol V Barium Sulfate Suspension

Failed Stability Specifications: Tagitol V Barium Sulfate Lot #65846 sampled at 10 months exhibited results above the upper specification for viscosity.

Terminated Stability / shelf life Bracco Diagnostics Inc NDC 32909-814-53 D-914-2013

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