Pure-Aid Allergy Relief, Diphenhydramine HCL Caplets, 25 mg, 20 caplets, Exclusively distributed by: Kareway Products Inc., Compton, CA --- UPC 8 56023 00158 2

FDA recall notice · announced July 3, 2013 · Kareway Product

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The 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

Notes

Distribution: Nationwide in the US: CA, OR, WA. Africa.
Lot/code information: Lot# 6781202 & 6781302
Quantity: 24,048 cartons
Status: Terminated
Products in this recall event:
- Pure-Aid Allergy Relief, Diphenhydramine HCL Caplets, 25 mg, 20 caplets, Exclusively distributed by: Kareway Products Inc., Compton, CA --- UPC 8 56023 00158 2 (D-620-2013)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.