Washington Homeopathic Recalls Ferrum Phosphoricum 6X Tablets for CGMP Deviations
Washington Homeopathic Products, Inc. is recalling Ferrum Phosphoricum 6X Tablets because they were not manufactured under current good manufacturing practices.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 and involves CGMP deviations without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Ferrum Phosphoricum 6X Tablets, 300-count bottles. The recall involves 462 bottles of the product, which was manufactured in India exclusively for the company.
The recall was initiated because the products were not manufactured under current good manufacturing practices (CGMP). The source text does not report any specific illnesses, injuries, or deaths associated with this recall.
The product was distributed nationwide throughout the United States, Canada, and Saudi Arabia. Consumers should check their inventory for Lot # BR18C281 and the barcode 7 40640 64198 9. If found, consumers should stop using the product and contact the recalling firm for instructions on disposal or return.
The recalled product
- Product
- Ferrum Phosphoricum 6X Tablets, 300-count bottle, 30g, Manufactured in India exclusively for: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV 25411, barcode 7 40640 64198 9.
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 462
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 (1)
- Lot # BR18C281
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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