Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer initiated recall of API product...

Date: April 3, 2017
Company: Medisca, 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 Medisca, Inc. directly.

Affected Products

ESTRADIOL, USP Bulk (Hemihydrate), in a) 25 g (NDC 38779-2261-04) and b) 100 g (NDC 38779-2261-05) bottles, Packed by MEDISCA INC. PLATTSBURGH, NY Product Code 2261

Quantity: N/A

Why Was This Recalled?

cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Medisca, Inc.

Medisca, Inc. has 6 total recalls tracked by RecallDetector.

Related Recalls

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