Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Mozobil (plerixafor injection) 24mg/1.2mL (20mg/mL) Recalled by Sanofi-Aventis U.S. LLC Due to Labeling: Incorrect or Missing Package Insert
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 Sanofi-Aventis U.S. LLC directly.
Affected Products
Mozobil (plerixafor injection) 24mg/1.2mL (20mg/mL), For Single Use Only, Rx Only, Manufactured by: Genzyme Corporation 500 Kendall Street, Cambridge, MA 02412 USA NDC: 0024-5862-01
Quantity: 2133 vials
Why Was This Recalled?
Labeling: Incorrect or Missing Package Insert
Where Was This Sold?
Nattionwide
About Sanofi-Aventis U.S. LLC
Sanofi-Aventis U.S. LLC has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report