# FDA recall D-620-2013

> **Kareway Product Inc** · Class II · drug recall initiated 2013-05-03.

## 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

## Distribution

Nationwide in the US: CA, OR, WA.    Africa.

## Key facts

- **Recall number:** D-620-2013
- **Recalling firm:** Kareway Product Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-05-03
- **Report date:** 2013-07-03
- **Termination date:** 2013-10-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Compton, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-620-2013

## Citation

> AI Analytics. FDA recall D-620-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-620-2013. Source: US FDA. Licensed CC0.

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