FDAFDA · Food and drugs·Recall number D-0812-2016
SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, Canada, NDC 65174-461-05
Published April 13, 2016 · Recall initiated: March 11, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Label Error on Declared Strength
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- SODIUM IODIDE I 131 DIAGNOSTIC
- Manufacturer
- Jubilant Draximage Inc
- Distributor
- Nationwide
- Lot
- Lot Number 1670123; Exp 04/16
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- Canada
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