Mozobil recall: Labeling Error
Mozobil (plerixafor injection) 24mg/1.2mL (20mg/mL), For Single Use Only, Rx Only, Manufactured by: Genzyme Corporation 500 Kendall Street, Cambridge…
Why was Mozobil recalled?
Labeling: Incorrect or Missing Package Insert
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 #: 5RZ001C, 5RZ001D; Exp. 04/18
- Product
- Mozobil (plerixafor injection) 24mg/1.2mL (20mg/mL), For Single Use Only, Rx Only, Manufactured by: Genzyme Corporation 500 Kendall Street, Cambridge…
- Recalling firm
- Sanofi-Aventis U.S. LLC
- Quantity
- 2133 vials
- Distribution
- Nattionwide
- Recall date
- May 17, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)