Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP Deviations: manufactured under practices which may result...
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 Nationwide Laboratories, LLC directly.
Affected Products
Salsalate Tablets, USP, 750 mg, packaged in a) 100 count bottles (NDC 42937-704-10); b) 500 count bottles (NDC 42937-704-18); and c) 1000 count bottles (NDC 42937-704-20); Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830.
Quantity: 2,514,500 tablets
Why Was This Recalled?
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Nationwide Laboratories, LLC
Nationwide Laboratories, LLC 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