Hetero USA Inc recalls Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway,…

Recall date

April 27, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0897-2017

FDA classification

Class III

Brand / firm

Hetero USA Inc

Sold / distributed

Nationwide

Why it was recalled

Presence of Foreign Substance: human hair melded into tablet.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, by Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, NDC 31722-778-01