FDA recall record

Volumex (Iodinated I 131 Albumin) Injection USP, 25 uCi per 1 mL syringe recall — FDA D-1136-2019

Lack of Assurance of Sterility: environmental monitoring report exceeds limits, therefore sterility cannot be assured.

Class IIclassification
D-1136-2019official record ID
Apr 24, 2019report date

Recall record at a glance

Official recordD-1136-2019
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIso-Tex Diagnostics, Inc.
Report dateApr 24, 2019
Recall initiation dateApr 15, 2019
Quantity54 1ml syringes
LocationAlvin, TX, United States

Official product description

Volumex (Iodinated I 131 Albumin) Injection USP, 25 uCi per 1 mL syringe, Rx Only, Manufactured for Daxor Corp., NY, NY; By: Iso-Tex Diagnostics, Inc.; NDC 50914-7720-8.

Why the product was recalled

Lack of Assurance of Sterility: environmental monitoring report exceeds limits, therefore sterility cannot be assured.

Distribution information

TN

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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