Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Draximage MAA (Kit for the preparation of Technnetium Tc 99m Recalled by Jubilant Draximage Inc Due to Lack of Assurance of Sterility: Out-of-specification test results...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Jubilant Draximage Inc directly.
Affected Products
Draximage MAA (Kit for the preparation of Technnetium Tc 99m Albumin Aggregate) 2.5 mg per vial, 30 glass vials per carton, Rx Only, Manufactured for Jubilant Draximage Inc. Kirkland, Canada, NDC 65174-270-30.
Quantity: 519 cartons/30 vials each
Why Was This Recalled?
Lack of Assurance of Sterility: Out-of-specification test results obtained for Endotoxin testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Jubilant Draximage Inc
Jubilant Draximage Inc has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report