SUCRETS Sore Throat & Cough Vapor Cherry lozenges — Class II drug recall D-1113-2015
Terminated recall by Medtech Products, Inc., reported 2015-06-10, distributed nationwide. Labeling: Label Mix-Up: An incorrect book label for Sucrets Sore Throat, Cough & Dry Mouth Honey Lemon lozenge
| Recall number | D-1113-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtech Products, Inc., Tarrytown, NY, United States |
| Recall initiated | 2015-05-21 |
| Classified | 2015-06-01 |
| Reported by FDA | 2015-06-10 |
| Terminated | 2018-06-06 |
| Distributed | Nationwide (US) |
| Quantity | 107,832 tins |
| Reason classes | labeling |
| Lot numbers | 09/17, 42451 |
Product
SUCRETS Sore Throat & Cough Vapor Cherry lozenges, 18-count tin, Dist. By: Insight Pharmaceuticals, LLC, Trevose, PA 19053-8433
Reason for recall
Labeling: Label Mix-Up: An incorrect book label for Sucrets Sore Throat, Cough & Dry Mouth Honey Lemon lozenges was applied to the underside of the Sucrets Sore Throat & Cough Vapor Cherry lozenges tin.
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-1113-2015. 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.