FDA Drug Recalls

Recalls / Class II

Class IID-0888-2021

Product

ZTE 1015 Formula, Contents 1000 ml, For Manufacturing Use only, REMEDY: Argentum Nitricum 10X, Rhus Toxicodendron 10X, Aurum Metallicum 10X, Iris Versicolor 10X, Lycopodium Clavatum 10X, Zincum Muriaticum 13X, Chromium Sulphuricum 10X, Manganum Metallicum 10X, Dilution Alcohol 20%, Manufactured for Optimal Health Dimensions, Manufactured by: Washington Homeopathic Products 260 JR Hawvernale Way, Berkeley Springs, WV, 25411,

Affected lot / code info
Lot # 25739, no expiry date

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
1 1/liter
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-0888-2021. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.