Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by Genzyme Corporation / Genzyme Biosurgery Due to Labeling: Incorrect or Missing Lot and/or Exp. Date

Date: August 4, 2016
Company: Genzyme Corporation / Genzyme Biosurgery
Status: Terminated
Source: FDA (Drug)

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 Genzyme Corporation / Genzyme Biosurgery directly.

Affected Products

Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial, Rx Only, For Subcutaneous Injection only, Manufactured by: Genzyme Corporation, 500 Kendall Street, Cambridge, MA 02142 A Sanofi Company Country of Origin : United Kingdom, NDC 0024-5862-01

Quantity: 9,530 vials

Why Was This Recalled?

Labeling: Incorrect or Missing Lot and/or Exp. Date

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Genzyme Corporation / Genzyme Biosurgery

Genzyme Corporation / Genzyme Biosurgery has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report