Jubilant Draximage Inc recalls SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, Can…
- Recall date
- March 11, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0812-2016
- FDA classification
- Class III
- Brand / firm
- Jubilant Draximage Inc
- Sold / distributed
- Nationwide
Why it was recalled
Labeling: Label Error on Declared Strength
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, Canada, NDC 65174-461-05
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