Recall Register

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Prestige Brands Holdings

FDA recalling firm · 3 enforcement events · 4 product records · 2014–2026 · NY

Prestige Brands Holdings has 3 FDA enforcement events on this register (4 product records) between 2014 and 2026: 2 drug and 1 food; the busiest year was 2014 with 1.

0% of its events are Class I; the most common class is Class II (2). 2 events are listed as ongoing; the recalling firm's address is in NY.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
29 Jul 2026CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3DrugClass II1Ongoing
18 Jun 2025Little Remedies¿ Honey Cough 4 FL OZ (118 mL)FoodClass II1Ongoing
25 Apr 2014PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold, (diphenhydramine HCl 6.25 mg and phenylephrine HCl 2.5 mg), 4 FL OZ (118 mL), Distributed by Medtech Products, Inc., Tarrytown,NY ---- UPC 814832013544DrugClass III2Terminated

By type and class

Drug2
Food1
Class II2
Class III1

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

14
16
18
20
22
24
26
Enforcement events for Prestige Brands Holdings by year initiated.

Questions and answers

How many FDA recalls has Prestige Brands Holdings had?

3 enforcement events (4 product records) on this register, 2014–2026: 2 drug, 1 food.

Are any Prestige Brands Holdings recalls ongoing?

2 events are listed as ongoing in the current openFDA export.

What class are Prestige Brands Holdings recalls?

2 Class II, 1 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.