Mycophenolate Mofetil recall: CGMP Deviations
Mycophenolate Mofetil, Bulk Powder, Quantity 1000 g, For prescription compounding use and medical manufacturing or processing only, Attix…
Why was Mycophenolate Mofetil recalled?
cGMP deviation; manufacturer is Not Registered with the Food and Drug Administration
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 Number: A3160A, Manufacturer batch number: 151201, Expiry November 2017
- Product
- Mycophenolate Mofetil, Bulk Powder, Quantity 1000 g, For prescription compounding use and medical manufacturing or processing only, Attix…
- Recalling firm
- Attix Pharmaceuticals Inc
- Quantity
- N/A
- Distribution
- CO
- Recall date
- June 29, 2016
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)