FDAClass IIISeptember 28, 2016

Mozobil recall: Labeling Error

Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial, Rx Only, For Subcutaneous Injection only, Manufactured by: Genzyme Corporation, 500…

Why was Mozobil recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot # 5RZ002; Exp. 04/18

Product
Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial, Rx Only, For Subcutaneous Injection only, Manufactured by: Genzyme Corporation, 500…
Recalling firm
Genzyme Corporation / Genzyme Biosurgery
Quantity
9,530 vials
Distribution
nationwide
Recall date
September 28, 2016
Classification
Class III
Status
Terminated
Agency
FDA (drug)
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