PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: June 14, 2017 Initiated: April 27, 2017 #D-0897-2017

Product Description

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

Reason for Recall

Presence of Foreign Substance: human hair melded into tablet.

Details

Recalling Firm
Hetero USA Inc
Units Affected
13,692 bottles
Distribution
Nationwide
Location
Piscataway, NJ

Frequently Asked Questions

What product 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. Recalled by Hetero USA Inc. Units affected: 13,692 bottles.
Why was this product recalled?
Presence of Foreign Substance: human hair melded into tablet.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 14, 2017. Severity: Low. Recall number: D-0897-2017.