Levetiracetam Oral Solution — Class II drug recall D-0099-2018
Terminated recall by Hetero Labs, Ltd. - Unit III, reported 2017-12-06, distributed in NJ. Presence of foreign substance (screw)
| Recall number | D-0099-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hetero Labs, Ltd. - Unit III, Hyderabad, N/A, India |
| Recall initiated | 2017-10-12 |
| Classified | 2017-11-29 |
| Reported by FDA | 2017-12-06 |
| Terminated | 2020-09-03 |
| Distributed | NJ |
| Quantity | 4,050 bottles |
| NDC | 31722-0574, 31722-0574-47 |
| Lot numbers | 02/19, E170346 |
Product
Levetiracetam Oral Solution, USP, 100 mg/mL, packaged in a 16 fl oz (473 mL) bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, By: Hetero, Hetero Labs Limited, Jeedimetla,Hyderabad - 500 055, India, NDC 31722-574-47
Reason for recall
Presence of foreign substance (screw)
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0099-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.