Class III โ€” Low Risk

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

Mycophenolate Mofetil Recalled by Attix Pharmaceuticals Inc Due to cGMP deviation; manufacturer is Not Registered with the...

Date: May 18, 2016
Company: Attix Pharmaceuticals Inc
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 Attix Pharmaceuticals Inc directly.

Affected Products

Mycophenolate Mofetil, Bulk Powder, Quantity 1000 g, For prescription compounding use and medical manufacturing or processing only, Attix Pharmaceuticals, Toronto, Canada

Quantity: N/A

Why Was This Recalled?

cGMP deviation; manufacturer is Not Registered with the Food and Drug Administration

Where Was This Sold?

This product was distributed to 1 state: CO

Affected (1 state)Not affected

About Attix Pharmaceuticals Inc

Attix Pharmaceuticals Inc has 1 total recall tracked by RecallDetector.

Related Recalls

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