FDA recall record

P & L Development Allergy Relief Diphenhydramine HCl 25 mg, Antihistamine, Dye-Free, 24 recall — FDA D-0694-2017

Subpotent: This product is being recalled due to low out of specification assay results at the 9 month time point.

Class IIIclassification
D-0694-2017official record ID
May 10, 2017report date

Recall record at a glance

Official recordD-0694-2017
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmP & L Development, LLC
Report dateMay 10, 2017
Recall initiation dateApr 17, 2017
Quantity369,012 cartons
LocationWestbury, NY, United States

Official product description

Allergy Relief Diphenhydramine HCl 25 mg, Antihistamine, Dye-Free, 24 Softgels, distributed under the following labels: (a) TopCare Allergy Relief, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007, NDC 36800-483-24, UPC 0-36800-39134-5; (b) Rexall Since 1903 Allergy Relief, PACKAGED FOR DOLGENCORP, LLC, 100 MISSION RIDGE GOODLETTSVILLE, TN 37072, UPC 3-59726-72025-0; (c) HyVee health Allergy Relief, DISTRIBUTED BY HY-VEE, INC. 5820 WESTOWN PARKWAY, WEST DES MOINES, IA 50266, NDC 42507-483-24, UPC 0-75450-12369-2; (d) up & up allergy relief, Distributed by Target Corporation, Minneapolis, MN 55403, NDC 11673-720-24, UPC 3-59726-72025-0; (e) smart sense allergy softgels, Distributed by Kmart Corporation, Hoffman Estates, IL 60179, NDC 49738-483-24, UPC 8-83967-39839-3.

Why the product was recalled

Subpotent: This product is being recalled due to low out of specification assay results at the 9 month time point.

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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