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.

Indomethacin Capsules Recalled by Hetero Labs, Ltd. - Unit III Due to Failed Tablet/Capsule Specifications: customer complaints of deformed, clumped,...

Date: July 18, 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

Indomethacin Capsules, USP, 50 mg, 100-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854; By: Hetero, Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India; NDC 31722-543-01.

Quantity: 18,288 bottles

Why Was This Recalled?

Failed Tablet/Capsule Specifications: customer complaints of deformed, clumped, misshaped, melted or stuck together capsules.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)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