Class II · Moderate risk
E-Z-HD (Barium Sulfate for Oral Suspension)
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 32909-0764-01 recalled?
E-Z-Hd · 24 BOTTLE in 1 CARTON (32909-764-01) / 340 g in 1 BOTTLE
Yes — this exact package was recalled
2 FDA recalls name the code 32909-0764-01 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.
- Active ingredient
- barium sulfate
- Strength
- BARIUM SULFATE 980 mg/g
- Form
- Powder, for Suspension · Oral
- Labeler
- E-Z-EM Canada Inc
- Type
- Human Prescription Drug
- Product code
- 32909-0764
Recalls naming this package
Class III · Low risk
E-Z-HD (barium sulfate)
Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.
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
- 32909-0727 See recall 1
- 32909-0770 E-Z-Paste 1
- 32909-0814 Tagitol V 1
- 32909-0945 See recall 1
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