FDA Drug recall D-498-2013
Lisinopril Tablets, USP, 30 mg, Rx only, 100 tablets, NDC 65862-041-01 Manufactured for: Aurobindo Pharma USA Inc. 2400 Route 130 North, Da…
- FDA Drug
- Class III
- terminated
- Published 2013-06-05
On 2013-06-05 the FDA classified a Class III recall of Lisinopril Tablets, USP, 30 mg, Rx only, 100 tablets, NDC 65862-041-01 Manufactured for: Aurobindo Pharma USA Inc. 2400 Route 130 North, Da… by Aurobindo Pharma Usa, citing labeling: Label Error on Declared Strength: Incorrect strength on side display panel of label.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-498-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-04-09 |
| Published | 2013-06-05 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Aurobindo Pharma Usa |
| Distribution | US |
Product
Lisinopril Tablets, USP, 30 mg, Rx only, 100 tablets, NDC 65862-041-01 Manufactured for: Aurobindo Pharma USA Inc. 2400 Route 130 North, Dayton, NJ 08810 Manufactured by: Aurobindo Pharma Limited Hyderabad- 500 072 India
Reason
Labeling: Label Error on Declared Strength: Incorrect strength on side display panel of label
Identifiers
| ndc | 65862-037-30 |
|---|---|
| ndc | 65862-037-01 |
| ndc | 65862-037-00 |
| ndc | 65862-037-05 |
| ndc | 65862-037-99 |
| ndc | 65862-038-30 |
| ndc | 65862-038-01 |
| ndc | 65862-038-00 |
| ndc | 65862-038-05 |
| ndc | 65862-038-99 |
| ndc | 65862-039-30 |
| ndc | 65862-039-01 |
| ndc | 65862-039-00 |
| ndc | 65862-039-05 |
| ndc | 65862-039-99 |
| ndc | 65862-040-30 |
| ndc | 65862-040-01 |
| ndc | 65862-040-00 |
| ndc | 65862-040-05 |
| ndc | 65862-040-99 |
| ndc | 65862-041-30 |
| ndc | 65862-041-01 |
| ndc | 65862-041-00 |
| ndc | 65862-041-05 |
| ndc | 65862-041-99 |
| ndc | 65862-042-30 |
| ndc | 65862-042-01 |
| ndc | 65862-042-00 |
| ndc | 65862-042-05 |
| ndc | 65862-042-99 |
| code_info | Lot KP3012001-A Exp.12/13 Lot KP3012002-A Exp.12/13 |
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-498-2013%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.