Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Ceftriaxone for Injection Recalled by Sandoz Inc Due to Labeling: Missing Label
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 Sandoz Inc directly.
Affected Products
Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwide, Inc., Lake Forest, Il 60045, USA, Made in Austria, NDC 0409-7332-01
Quantity: 139,430 vials
Why Was This Recalled?
Labeling: Missing Label
Where Was This Sold?
This product was distributed to 1 state: WI
About Sandoz Inc
Sandoz Inc has 30 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report