FDA recall record

Washington Homeopathic Products Z-103 GU DETOXING. Contents 1000ml 20% Alcohol. WHP recall — FDA D-0879-2021

Out-of-specification test results obtained for identification testing based on HPTLC analysis.

Class IIclassification
D-0879-2021official record ID
Oct 6, 2021report date

Recall record at a glance

Official recordD-0879-2021
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmWashington Homeopathic Products, Inc.
Report dateOct 6, 2021
Recall initiation dateAug 20, 2021
Quantity2/1 Liter bottles
LocationBerkeley Springs, WV, United States

Official product description

Z-103 GU DETOXING. Contents 1000ml 20% Alcohol. WHP Homeopathic Medicine. For Manufacturing Use Only, REMEDY: Agrimonia Eupatoria 24X, Alfalfa 24X, Althaea Officinalis 24X, Avena Sativa 24X, Boldo 24X, Carduus Marianus 24X, Chioanathus Virginica 24X, Cynara Scolymus 24X, Iria Versicolor 24X, Millefolium 24X, Rumex Crispus 24X, Selenium Metallicum 12X, Selenium Metallicum 60X, Solidago Virgaurea 12X, Solidago Virgaurea 24X, Solidago Virgaurea 60X, Spiraea Ulmaira 24X, Taraxacum Officinale 24X, Urtica Dioica 24X, Uva-Ursi 24X, Zincum Muriaticum 13X, Zincum Mruiaticum 30X, Dilution Alcohol 20%. Manufactured for Optimal Health Dimensi. RX Only, Manufactured by Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV, 25411.

Why the product was recalled

Out-of-specification test results obtained for identification testing based on HPTLC analysis.

Distribution information

Distributed Nationwide in the USA

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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