FDA recall record

Rohto Cooling Eye Drops Max Strength recall — FDA D-0717-2026

Lack of Assurance of Sterility

Class IIclassification
D-0717-2026official record ID
Jul 29, 2026report date

Recall record at a glance

Official recordD-0717-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmRohto-Mentholatum (Vietnam) Co., Ltd.
Report dateJul 29, 2026
Recall initiation dateJul 14, 2026
Quantity499,673 cartons
LocationHo Chi Minh, N/A, Vietnam

Official product description

Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 80 0.2%), Sterile, TWIN PACK, 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011210, NDC 10742-8158-2

Why the product was recalled

Lack of Assurance of Sterility

Distribution information

Nationwide within the United States

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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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