Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Isoniazid Tablets Recalled by West-Ward Pharmaceutical Corp. Due to Failed Dissolution Specifications: Stability lots cannot support dissolution...
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 West-Ward Pharmaceutical Corp. directly.
Affected Products
Isoniazid Tablets, USP, 300 mg, Rx only, packaged in a) 100-count bottles, NDC 0143-1261-01, b) 1000-count bottles, NDC 0143-1261-10, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724; c) 30-count bottles, NDC 61748-013-30, d) 100-count bottles, NDC 61748-013-01, e) 1000-count bottles, NDC 61748-013-10, Mfd. for: VersaPharm Incorporated, Marietta, GA 30062; Mfd. by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.
Quantity: a) 17,347 bottles, b) 3,015 bottles, c) 1,334 bottles, d) 5,651 bottles, e) 210 bottles
Why Was This Recalled?
Failed Dissolution Specifications: Stability lots cannot support dissolution past the 36 month time point.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About West-Ward Pharmaceutical Corp.
West-Ward Pharmaceutical Corp. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report