FDA Drug recall D-0897-2017
Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, by Hetero…
- FDA Drug
- Class III
- terminated
- Published 2017-06-14
On 2017-06-14 the FDA classified a Class III recall of Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, by Hetero… by Hetero Usa, citing presence of Foreign Substance: human hair melded into tablet.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0897-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-04-27 |
| Published | 2017-06-14 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hetero Usa |
| Distribution | US |
Product
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
Presence of Foreign Substance: human hair melded into tablet.
Identifiers
| ndc | 31722-777-01 |
|---|---|
| ndc | 31722-777-05 |
| ndc | 31722-778-01 |
| ndc | 31722-778-05 |
| code_info | Lot # ACY16075 Exp. 09/2018 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0897-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.