CLASS II Drug recall · Reported 6 Oct 2021 · FDA Enforcement Report
ZTE-105 Formula Gentle Detoxing recalled by Washington Homeopathic
Washington Homeopathic Products is recalling ZTE-105 Formula Gentle Detoxing, distributed nationwide in the US. The recall was initiated on 20 Aug 2021 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0858-2021
- FDA event ID
- 88528
- Recalling firm
- Washington Homeopathic Products, Berkeley Springs, WV
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 20 Aug 2021
- FDA classified
- 29 Sep 2021
- Reported
- 6 Oct 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
Timeline
| 20 Aug 2021 | Recall initiated by company | |
| 29 Sep 2021 | Classified by FDA | +40 days |
| 6 Oct 2021 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Product as listed by the FDA
ZTE-105 Formula Gentle Detoxing. Contents 1000 mL, RX Only, REMEDY: Bryoni Alba 10X, Chelidonium Majus 10X, Carduus Marianus 10X, Dolichos Pruriens 10X, Solidago Vigaurea 10X, Alfalfa 10X, Boldo 10X, Cynara Scolymus 10X, Zincum Muriaticum 13X, Chromium Sulphuricum 10X, Manganum Metallicum 10X, Dilution Alcohol 20%. WHP Homeopathic Medicine. For Manufacturing Use Only, Manufactured for Optimal Health Dimensi. Manufactured By: Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV, 25411.
Where it was distributed
Distributed Nationwide in the USA
Questions about this recall
Why was it recalled?
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Which lots are affected?
Lot # 25950, 26933, Exp 8/17/2026
Where was it sold?
Distributed Nationwide in the USA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
38 other products · FDA event 88528This product is part of a recall event; the main page for the event is Occular Allergy Blend 87% Alcohol recalled by Washington Homeopathic.