Cipla USA recalls 1000mg Lanthanum Carbonate chewable tablets due to hardness test failure. This may affect tablet integrity and safety. Check your Rx-only medication packaging for the recall.
Failed stability specifications: Out of specification for hardness test
Cipla USA is recalling Lanthanum Carbonate chewable tablets (1000mg) that failed stability testing for hardness. This could mean the tablets might break or crumble, potentially causing injury if taken.
The tablets failed hardness testing, meaning they may crumble or break more easily than expected. This could lead to the tablets not dissolving properly or causing injury if they break during swallowing.
Patients prescribed Lanthanum Carbonate chewable tablets (1000mg) by a doctor. Those with the specific packaging (10x9 bottles per patient pack carton) are most at risk.
Check for the product name 'Lanthanum Carbonate chewable tablets, 1000mg', 10x9 bottles per patient pack carton, and Rx-only labeling. The lot number NB240315 was manufactured until December 31, 2025.
Look for the product name, dosage, and packaging details as listed in the recall notice.
The recall indicates the tablets failed hardness testing, but the product is still safe to take if used as directed. However, the manufacturer recommends checking for the recall.
Check for the specific packaging: Lanthanum Carbonate chewable tablets, 1000mg, 10x9 bottles per patient pack carton, and Rx-only labeling.
The recall does not specify a remedy, so contact your doctor or pharmacist for guidance on safe alternatives.
We’ve drafted a message you can send Cipla to request your refund or repair — edit it as you like.
Subject: Recall D-0217-2026 — Cipla Cipla Hello, I own a Cipla that is covered by recall D-0217-2026 from Cipla. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
