FDA Drug Recalls

Recalls / Active ingredient / Human Serum Albumin I-131

Human Serum Albumin I-131

2 FDA drug recalls involving the active ingredient “Human Serum Albumin I-131.

DateClassProductFirm
2019-04-15Class IIVolumex (Iodinated I 131 Albumin) Injection USP, 25 uCi per 1 mL syringe, Rx Only, Manufactured for Daxor CorpIso-Tex Diagnostics, Inc
2019-03-11Class IIVolumex (Iodinated I 131 Albumin) Injection USP, 25 uCi per 1 mL syringe, Rx Only, Manufactured for Daxor CorpIso-Tex Diagnostics, Inc