Melatonin Control- Released Tablets — Class III food recall F-1202-2015
Terminated recall by HVL, LLC, reported 2015-02-18, distributed nationwide. Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin.
| Recall number | F-1202-2015 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | HVL, LLC, Pittsburgh, PA, United States |
| Recall initiated | 2015-01-12 |
| Classified | 2015-02-12 |
| Reported by FDA | 2015-02-18 |
| Terminated | 2015-07-28 |
| Distributed | Nationwide (US) |
| Quantity | 278 |
| Lot numbers | 50032151 |
| Expiration dates | 2015-12-20 |
Product
Melatonin Control- Released Tablets, 60 tablets, in plastic bottles, Manufactured by Douglas Laboratories, Pittsburgh, PA.
Reason for recall
Bottles contained a vegetarian digestive enzyme dietary supplement instead of melatonin.
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/F-1202-2015. 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.