Prestige Brands Holdings Recalls

Overview of recall records associated with Prestige Brands Holdings, including dates, categories and classifications where available.

3recall records

Aug 19, 2026latest record date

Jun 4, 2014earliest record date

Recall history in this database

Classification mix: Class III: 2, Class II: 1.

DrugAug 19, 2026

CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by recall — FDA D-0766-2026

Lack of assurance of sterility. The recall is due to potential contamination

Class IIFDA: OngoingPrestige Brands Holdings

DrugJun 4, 2014

Prestige Brands Holdings PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold recall — FDA D-1352-2014

Presence of Precipitate; small amounts of diphenhydramine precipitated out of solution

Class IIIFDA: TerminatedPrestige Brands Holdings

DrugJun 4, 2014

Prestige Brands Holdings PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold recall — FDA D-1353-2014

Presence of Precipitate; small amounts of diphenhydramine precipitated out of solution

Class IIIFDA: TerminatedPrestige Brands Holdings

Understanding this recall history

This page summarizes recall records in which the official source identifies Prestige Brands Holdings 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.