Jubilant Draximage Inc recalls SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, Cana
Recalled April 13, 2016 · FDA recall D-0812-2016 · Jubilant Draximage
Hazard
Labeling: Label Error on Declared Strength · FDA Class III
Units
90 vials (450 capsules)
Sold at
Nationwide
Description
Labeling: Label Error on Declared Strength
Product
SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, Canada, NDC 65174-461-05
Manufacturer(s)
Jubilant Draximage Inc
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →