PlainRecalls
FDA Drug Moderate Class II Terminated

Haloderm Homeopathic Blend, For Manufacturing Use Only, 1,000 ml 20% Alcohol, Contains: Dulcamara 10x, Nitricum Acidum 12x, Thuja Occidentalis 10x, Antimonium Crudum 12x, Calcarea Cadbonica 12x, Silicea 12x, WHP Homeopathic Medicine, FOr Manufacturing Use Only. 1.957 kg Lactose Manufactured by Wasington Homeopathic Products 260 JR Hawvermale Way, Berkeley Springs WV 25411. Marketed by: Health Specialty

Reported: October 6, 2021 Initiated: August 20, 2021 #D-0861-2021

Product Description

Haloderm Homeopathic Blend, For Manufacturing Use Only, 1,000 ml 20% Alcohol, Contains: Dulcamara 10x, Nitricum Acidum 12x, Thuja Occidentalis 10x, Antimonium Crudum 12x, Calcarea Cadbonica 12x, Silicea 12x, WHP Homeopathic Medicine, FOr Manufacturing Use Only. 1.957 kg Lactose Manufactured by Wasington Homeopathic Products 260 JR Hawvermale Way, Berkeley Springs WV 25411. Marketed by: Health Specialty

Reason for Recall

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

Details

Units Affected
3 Liter bottles
Distribution
Distributed Nationwide in the USA
Location
Berkeley Springs, WV

Frequently Asked Questions

What product was recalled?
Haloderm Homeopathic Blend, For Manufacturing Use Only, 1,000 ml 20% Alcohol, Contains: Dulcamara 10x, Nitricum Acidum 12x, Thuja Occidentalis 10x, Antimonium Crudum 12x, Calcarea Cadbonica 12x, Silicea 12x, WHP Homeopathic Medicine, FOr Manufacturing Use Only. 1.957 kg Lactose Manufactured by Wasington Homeopathic Products 260 JR Hawvermale Way, Berkeley Springs WV 25411. Marketed by: Health Specialty. Recalled by Washington Homeopathic Products, Inc.. Units affected: 3 Liter bottles.
Why was this product recalled?
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 6, 2021. Severity: Moderate. Recall number: D-0861-2021.