Hi-Tech Pharmaceuticals recalled 85,950 units of its Flexible Joint Formula on August 6, 2025. The recall follows concerns over unapproved drug claims associated with the product. It was distributed across 50 states and U.S. territories.
Unapproved Drug Claims.
Consumers who have purchased this product should not consume it. Contact Hi-Tech Pharmaceuticals Inc. for refund or replacement information. Notification method: Letter
The recalled product is Hi-Tech Pharmaceuticals Flexible Joint Formula, which contains 240 capsules per bottle. The specific lot affected is 405310805 with an expiration date of July 28. The product was shipped to various states including California, Florida, and New York.
The recall stems from unapproved drug claims related to the product's ability to support tendons, muscles, and cartilage. This classification falls under Class III, indicating the potential for harm due to misleading claims but not immediate danger.
No specific incidents, injuries, or deaths have been reported in relation to this recall. The recall is precautionary due to the product's misleading claims.
Consumers should stop using the product immediately. Contact Hi-Tech Pharmaceuticals for refund or replacement information.
Consumers can reach Hi-Tech Pharmaceuticals at their official website or through customer service for more details on the recall.
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