Recalls / Class II

Class IID-0870-2021

Product

La Core LCL-2-0191 Blend, 149,980ml 20% Alcohol, WHP Homeopathic Medicine, For Manufacturing Only, Liter LCL-2-0191-Bend: 12% Lycopodium Clavatum 10X, 12% Carbo Vegetabilis 16X, 12% Natrum Muriaticum 9X, 12% Calcarea Carbonica 12X, 10% Hypothalamus 30X, 6% Pituitarum Posterium 12X, 6% Pituitarum Posterium 30C, 3% Natrum Phosphoricum 12X, 3% Graphites 30X, 3# Agnus Castus 6X, 3% Thiosinaminum 8X, 3% Phytolacca Decandra 12X, 3% Magnesia Phosphorica 10X, 3% Ornithogalum Umbellatum 6X, 3% Chelidonium Majus 6X, 3% Quercus Robur 14X, 3% Nux Vomica 30X, Manufactured by Washington Homeopathic Products 260 JR Hawvermale Way, Berkeley Springs, WV, 25411.

Affected lot / code info

Lot # 27861, Exp 8/17/2026

Why it was recalled

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

Recalling firm

Firm

Washington Homeopathic Products, Inc.

Notification channel

Letter

Type

Voluntary: Firm initiated

Address

260 J R Hawvermale Way, N/A, Berkeley Springs, West Virginia 25411-6957

Distribution

Quantity

2/149,980 mL bottles

Distribution pattern

Distributed Nationwide in the USA

Timeline

Recall initiated

2021-08-20

FDA classified

2021-09-29

Posted by FDA

2021-10-06

Terminated

2022-06-21

Status

Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0870-2021. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.