Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Lamivudine Tablets Recalled by American Health Packaging Due to Labeling: Incorrect or Missing Package Insert; an error...
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 American Health Packaging directly.
Affected Products
Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC: 60687-362-11), Distributed by American Health Packaging, Columbus, OH
Quantity: 60 cartons
Why Was This Recalled?
Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms and Strengths section of the insert that incorrectly lists the tablet description coding for the tablets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About American Health Packaging
American Health Packaging has 56 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report