Cipla USA recalled 1,180 boxes of Lanthanum Carbonate chewable tablets on October 24, 2025. The recall follows a failure to meet stability specifications for hardness tests. Consumers and healthcare providers must stop using the product immediately.
Failed stability specifications: Out of specification for hardness test
Consumers and healthcare providers should stop using this product immediately. Contact Cipla USA, Inc. or your healthcare provider for guidance. Notification method: N/A
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The recall includes Lanthanum Carbonate chewable tablets, 1000mg. The affected lot number is NB240315, with an expiration date of December 31, 2025. The product was distributed nationwide in the USA.
The recalled Lanthanum Carbonate tablets failed stability specifications, specifically the hardness test. This may impact the effectiveness of the medication, posing potential health risks.
No incidents or injuries have been reported as a result of this recall. However, the high hazard level indicates a significant risk of reduced effectiveness.
Stop using the recalled tablets immediately. Contact Cipla USA, Inc. or your healthcare provider for further guidance.
For questions, consumers can reach Cipla USA, Inc. at their office in Warren, NJ. Additional information is available on the FDA website.
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