Class II · Moderate risk
Volumex (Iodinated I 131 Albumin)
Lack of Assurance of Sterility: environmental monitoring report exceeds limits, therefore sterility cannot be assured.
National Drug Code
Is NDC 50914-7720-08 recalled?
Volumex · 1 mL in 1 SYRINGE, PLASTIC (50914-7720-8)
Yes — this exact package was recalled
2 FDA recalls name the code 50914-7720-08 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
- Iodinated I-131 Albumin
- Strength
- HUMAN SERUM ALBUMIN I-131 .025 mCi/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Iso-Tex Diagnostics, Inc.
- Type
- Human Prescription Drug
- Product code
- 50914-7720
Recalls naming this package
Class II · Moderate risk
Volumex (Iodinated I 131 Albumin)
Lack of Assurance of Sterility: preliminary environmental monitoring report exceeds limits, therefore sterility cannot be assured.
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.
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