Drug recall D-0812-2016
Product
SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, Canada, NDC 65174-461-05
Reason for recall
Labeling: Label Error on Declared Strength
Lots and codes
Lot Number 1670123; Exp 04/16
Recall details
- Recalling firm
- Jubilant Draximage Inc, Kirkland, N/A
- Quantity
- 90 vials (450 capsules)
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 11, 2016
- Terminated
- August 7, 2017
Related products
- Sodium Iodide I 131 Diagnostic – drug information
- NDC 65174-461 Sodium Iodide I 131 Diagnostic · Sodium Iodide I-131 100 mCi/1 · Jubilant DraxImage Inc., dba Jubilant Radiopharma