Every recall we track for Lannett Company Inc. — 15 in all — plus the complaints and injury reports the public filed about them.
a ~150-character meta description summarising the recall.
Lannett recalls 1,000 mg niacin extended-release tablets due to failed dissolution testing. This may affect medication effectiveness. Contact Lannett for details.
Lannett recalls Primidone 250mg tablets due to trace acemetacin contamination. Affected lots have specific expiration dates and are prescription-only.
Lannett Company recalls 1,000 mg niacin extended-release tablets (Rx only) due to failed dissolution specifications. This may affect safety in normal use. Check NDC and lot numbers for affected batches.
Lannett recalls 10mg ADHD medication bottles with foreign tablets. Consumers should check for 5mg tablets in 100-count bottles. No immediate action needed but verify product details.
Lannett recalls 40mg Lisdexamfetamine capsules due to label mix-up with 30mg strength. This could lead to incorrect dosing if taken without proper label check.
Lannett recalls 10mg Lisdexamfetamine Dimesylate capsules due to failed content uniformity. This affects Rx-only products with specific NDC and lot numbers. Consumers should contact the manufacturer for details.
Lannett recalls 1000-capsule bottles of Triamterene and Hydrochlorothiazide (37.5mg/25mg) due to failed impurity specifications. Rx-only medication distributed in specific lots from December 2022 to January 2023.
Lannett recalls triamterene and hydrochlorothiazide capsules (37.5 mg/25 mg) due to failed impurity and degradation specifications. Rx-only capsules with NDC 0527-1632-01 or 0527-1632-10 lots 21000279A (exp 01/2023) and 20256320A (12/2022) are affected.
Lannett recalls Diazepam Oral Solution bottles with specific lot numbers due to impurities that may cause harm. Consumers should contact the manufacturer for details.
