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.

Aripiprazole Tablets Recalled by Hetero Labs, Ltd. - Unit III Due to CGMP Deviations: lot made with active pharmaceutical ingredient...

Date: January 10, 2018
Company: Hetero Labs, Ltd. - Unit III
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 Labs, Ltd. - Unit III directly.

Affected Products

Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, By; Hetero Hetero Labs Limited Unit V Polepallly Jadcheria Mahaboob Nagar - 509 301 India, NDC 31722-827-30

Quantity: 3000 bottles

Why Was This Recalled?

CGMP Deviations: lot made with active pharmaceutical ingredient that did not meet all its intended specifications.

Where Was This Sold?

This product was distributed to 1 state: NJ

Affected (1 state)Not affected

About Hetero Labs, Ltd. - Unit III

Hetero Labs, Ltd. - Unit III has 5 total recalls tracked by RecallDetector.

Related Recalls

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