Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Limbrel250 (flavocoxid and citrated zinc bisglycinate) 250 mg/50 mg capsules Recalled by Primus Pharmaceuticals, Inc. Due to Marketed Without An Approved NDA/ANDA: Based on the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Primus Pharmaceuticals, Inc. directly.
Affected Products
Limbrel250 (flavocoxid and citrated zinc bisglycinate) 250 mg/50 mg capsules, 60-count bottle, Rx only, Manufactured for: Primus Pharmaceuticals, Inc., Scottsdale, AZ 85253; Manufactured by: Cornerstone Research and Development, Ogden, UT 84404, NDC 68040-605-16.
Quantity: 4,006 bottles
Why Was This Recalled?
Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these products are unapproved drugs for which the safety and efficacy have not been established and, therefore, subject to recall.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Primus Pharmaceuticals, Inc.
Primus Pharmaceuticals, Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report