FDA Drug Recalls

Recalls / Class II

Class IID-0879-2021

Product

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.

Affected lot / code info
Lot # 26364, Exp 8/17/2026

Why it was recalled

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

Recalling firm

Firm
Washington Homeopathic Products, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
260 J R Hawvermale Way, N/A, Berkeley Springs, West Virginia 25411-6957

Distribution

Quantity
2/1 Liter bottles
Distribution pattern
Distributed Nationwide in the USA

Timeline

Recall initiated
2021-08-20
FDA classified
2021-09-29
Posted by FDA
2021-10-06
Terminated
2022-06-21
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0879-2021. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.