Pure-Aid Allergy Relief — Class II drug recall D-620-2013
Terminated recall by Kareway Product Inc, reported 2013-07-03, distributed nationwide. Labeling: Not Elsewhere Classified; foil label on immediate blister pack indicates active ingredient as Chlorp
| Recall number | D-620-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Kareway Product Inc, Compton, CA, United States |
| Recall initiated | 2013-05-03 |
| Classified | 2013-06-26 |
| Reported by FDA | 2013-07-03 |
| Terminated | 2013-10-28 |
| Distributed | Nationwide (US) |
| Quantity | 24,048 cartons |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00856023001582 |
| Lot numbers | 6781202, 6781302 |
Product
Pure-Aid Allergy Relief, Diphenhydramine HCL Caplets, 25 mg, 20 caplets, Exclusively distributed by: Kareway Products Inc., Compton, CA --- UPC 8 56023 00158 2
Reason for recall
Labeling: Not Elsewhere Classified; foil label on immediate blister pack indicates active ingredient as Chlorpheniramine rather than Diphenhydramine
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-620-2013. 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.