RecallRadar

FDA Drug recall D-0883-2021

Z-1050 Formula Hepatodetox

On 2021-10-06 the FDA classified a Class II recall of Z-1050 Formula Hepatodetox by Washington Homeopathic Products, citing out-of-specification test results obtained for identification testing based on HPTLC analysis.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0883-2021
ClassificationClass II
Statusterminated
Initiated2021-08-20
Published2021-10-06
Last updated2026-09-13 11:52 UTC
CompanyWashington Homeopathic Products
DistributionUS

Product

Z-1050 Formula Hepatodetox. Contents 1000ml. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY: Cholesterinum 10X, Avena Sativa 12X, Cynara Scolymos 12X, Phosphorus 12X, Oroticum Acidum 13X, Aesculus Hipposcastanum 24X, Carduus Marianus 24X, Chelidonium Majus 24X, Cimicifuga Racemosa 24X, Cinchona Officinalis 24X, Colocynthis 24X, Histaminum Hydrochloricum 24X, Lycopodium Clavatum 24X, Sulphur 24X, Tataxacum Officinale 24X, Veratrum Album 24X, Sepia 30X, Strontium Carbonicum 30X, Dilution Alcohol 20%. Manufactured for Optimal Health Dimensions. RX Only. anufactured by Washington Homeopathic Products, Inc. 260 JR Hawvermale Way, Berkeley Springs, WV, 25411.

Reason

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

Identifiers

code_infoLot # 26071, 28180, Exp 8/17/2026

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0883-2021%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.