# FDA recall D-0888-2021

> **Washington Homeopathic Products, Inc.** · Class II · drug recall initiated 2021-08-20.

## 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,

## Reason for recall

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

## Distribution

Distributed Nationwide in the USA

## Key facts

- **Recall number:** D-0888-2021
- **Recalling firm:** Washington Homeopathic Products, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-08-20
- **Report date:** 2021-10-06
- **Termination date:** 2022-06-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Berkeley Springs, WV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0888-2021

## Citation

> AI Analytics. FDA recall D-0888-2021. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/D-0888-2021. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
