FDA recall record

REMEDY ANTIFUNGAL Clinical TREAT Antifungal Powder, Vanilla Scent, 3 OZ (85 g) tube, Active recall — FDA D-0091-2024

CGMP deviations: the product was shipped from the Manufacturer to a Medline warehouse and released to stock while it was still under investigation for low…

Class IIclassification
D-0091-2024official record ID
Nov 15, 2023report date

Recall record at a glance

Official recordD-0091-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMEDLINE INDUSTRIES, LP - Northfield
Report dateNov 15, 2023
Recall initiation dateOct 4, 2023
LocationNorthfield, IL, United States

Official product description

Clinical TREAT Antifungal Powder, Vanilla Scent, 3 OZ (85 g) tube, Active Ingredient: Miconazole Nitrate 2.0% w/w Antifungal, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA, NDC: 53329-169-79

Why the product was recalled

CGMP deviations: the product was shipped from the Manufacturer to a Medline warehouse and released to stock while it was still under investigation for low assay results on the active ingredient miconazole nitrate.

Distribution information

Nationwide

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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