DermaZinc Spray — Class III drug recall D-1380-2012
Terminated recall by Quadrant Chemical Corporation, reported 2012-06-20, distributed in ME. Subpotent (Single Ingredient Drug): The firm is recalling the product because the product is subpotent and doe
| Recall number | D-1380-2012 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Quadrant Chemical Corporation, Garland, TX, United States |
| Recall initiated | 2012-03-20 |
| Classified | 2012-06-14 |
| Reported by FDA | 2012-06-20 |
| Terminated | 2012-09-13 |
| Distributed | ME |
| Quantity | 4,800 bottles |
| Reason classes | labeling, potency |
| Lot numbers | 022110-01 |
Product
DermaZinc Spray, 0.25% zinc pyritione, topical OTC, 4 fl oz bottle Distributed By: Dermallogix Partners, Inc. Scarborough, ME 04070
Reason for recall
Subpotent (Single Ingredient Drug): The firm is recalling the product because the product is subpotent and does not meet the labeled 0.25% zinc pyrithione level.
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-1380-2012. 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.