Class III โ€” Low Risk

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

Finasteride Tablets Recalled by Hetero Drugs Ltd. - Unit 1 Due to Failed Tablet/Capsule Specification: Tablets were found to be...

Date: December 29, 2016
Company: Hetero Drugs Ltd. - Unit 1
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 Hetero Drugs Ltd. - Unit 1 directly.

Affected Products

Finasteride Tablets, USP 5 mg, 90-count bottles, Rx only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs, Unit V Polepally, Jadcheria, Mahaboob Nagar - 509 301, India Limited NDC 31722-525-90

Quantity: 20,412 units

Why Was This Recalled?

Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.

Where Was This Sold?

This product was distributed to 1 state: NJ

Affected (1 state)Not affected

About Hetero Drugs Ltd. - Unit 1

Hetero Drugs Ltd. - Unit 1 has 1 total recall tracked by RecallDetector.

Related Recalls

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