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.
Overview of recall records associated with P & L Development, LLC, including dates, categories and classifications where available.
Classification mix: Class III: 1.
Subpotent: This product is being recalled due to low out of specification assay results at the 9 month time point.
This page summarizes recall records in which the official source identifies P & L Development, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.