Homeopathic Tuberculinum Drug Recalled for Manufacturing Practice Deviations
Washington Homeopathic Products is recalling Tuberculinum homeopathic drug in multiple potencies due to manufacturing practice deviations. The voluntary recall affects product distributed nationwide.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II voluntary recall initiated by the manufacturer due to manufacturing practice deviations. No illnesses or injuries have been reported, and the specific nature of the manufacturing deviations is not detailed in the source, making this a precautionary quality-control recall rather than an active safety threat.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Tuberculinum homeopathic drug available in potencies of 1X, 12X, 24X, 30X, and 1M in liquid pellet form. This prescription-only product was distributed nationwide across the United States. The recalled lot numbers are 20388 and 22728.
The recall was initiated due to current Good Manufacturing Practice (cGMP) deviations discovered during manufacturing operations. The manufacturer voluntarily initiated this recall in response to these deviations.
The recall was terminated on May 25, 2023, indicating that the firm completed corrective actions.
The recalled product
- Product
- Tuberculinum, Potency: 1X, 12X, 24X, 30X, 1M, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 15
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot# 20388
- 22728
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 17 recalled by Washington Homeopathic Products, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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