Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
NABUMETONE Tablets USP Recalled by Teva Pharmaceuticals USA Due to Labeling: Not Elsewhere Classified: Lack of leaflets and...
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 Teva Pharmaceuticals USA directly.
Affected Products
NABUMETONE Tablets USP, 750 mg, 100 count bottle,Teva Pharmaceutical Industries Ltd., Jerusalem, 91010, ISRAEL
Quantity: 576 bottles
Why Was This Recalled?
Labeling: Not Elsewhere Classified: Lack of leaflets and approved labels on bottles.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA
Teva Pharmaceuticals USA has 196 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report