Methylphenidate Hydrochloride Oral Solution 5mg per 5mL — Class III drug recall D-0142-2020
Terminated recall by KVK-Tech, Inc., reported 2019-10-23, distributed nationwide. Presence of Foreign Substance; Fiber particles.
| Recall number | D-0142-2020 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | KVK-Tech, Inc., Newtown, PA, United States |
| Recall initiated | 2019-10-04 |
| Classified | 2019-10-15 |
| Reported by FDA | 2019-10-23 |
| Terminated | 2020-04-20 |
| Distributed | Nationwide (US) |
| Quantity | 384 bottles |
| NDC | 10702-0163-50 |
| Lot numbers | 15315A |
| Expiration dates | 2021-02 |
Product
Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown, PA 18940, NDC 10702-0163-50.
Reason for recall
Presence of Foreign Substance; Fiber particles.
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-0142-2020. 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.