D-0881-2021 Class II Terminated
FDA drug recall D-0881-2021 was initiated by Washington Homeopathic Products, Inc. on August 20, 2021 and is designated Class II. Reason for recall: Out-of-specification test results obtained for identification testing based on HPTLC analysis. The recall status is terminated (terminated June 21, 2022). Affected quantity: 1 1/Liter bottle.
Recall Details
- Product Type
- Drugs
- Report Date
- October 6, 2021
- Initiation Date
- August 20, 2021
- Termination Date
- June 21, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 1/Liter bottle
Product Description
ZTE-1020 Formula. Contents 1000ml. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY: Aurum Metallicum 10X, Crataegus Oxyacantha 10X, Baryta Carbonica 10X, Digitalis Purpurea 10X, Zincum Muriaticum 13X, Chromium Sulphuricum 10X, Manganum Metallicum 10X, Dilution Alcohol 20%. Manufactured for Optimal Health Dimensions. RX Only, Manufactured by Washington Homeopathic Products, Inc. 260 JR Hawvermale Way, Berkeley Springs, WV, 25411.
Reason for Recall
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Distribution Pattern
Distributed Nationwide in the USA
Code Information
Lot # 25740, Exp 8/17/2026