Washington Homeopathic Products Recalls Pareira Tincture for Manufacturing Deviations
Washington Homeopathic Products is recalling Pareira (Brava) 1X Tincture because it was not manufactured under current good manufacturing practices.
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: The recall is classified as FDA Class II, which typically indicates a situation where use of the product may cause temporary or medically reversible health consequences. The source text does not report specific injuries or illnesses, aligning with a moderate severity rating for manufacturing deviations.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Pareira (Brava) 1X Tincture, 50 mL bottles. The recall was initiated because the products were not manufactured under current good manufacturing practices (CGMP).
The affected product is identified by Lot # 101471 and an expiration date of 08/01/2020. The product was distributed nationwide in the United States, as well as in Canada and Saudi Arabia.
Consumers who have this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Pareira (Brava) 1X Tincture, 50 mL bottle, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic Tincture
- Hazard
- Affected units
- 1
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 #: 101471
- Exp 08/01/2020
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 16 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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