Class III โ€” Low Risk

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

Fabior (tazarotene) Foam Recalled by Mayne Pharma Inc Due to Superpotent Drug: High out of specification results for...

Date: March 21, 2018
Company: Mayne Pharma 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 Mayne Pharma Inc directly.

Affected Products

Fabior (tazarotene) Foam, 0.1%, 100 grams can, Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834; NDC 51862-295-10.

Quantity: 3312 cans

Why Was This Recalled?

Superpotent Drug: High out of specification results for tazarotene assay at the 9-month stability time point.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Mayne Pharma Inc

Mayne Pharma Inc has 6 total recalls tracked by RecallDetector.

Related Recalls

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