Lanthanum Carbonate recalls
The FDA has published 4 recalls involving Lanthanum Carbonate since 2024. The latest was reported on 17 Dec 2025. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls4since 2024
Last 12 months2reported
Class I00% of total
Ongoing4latest 17 Dec 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 100%Class III 0 0%
Why lanthanum carbonate is recalled
Companies
By year
Ongoing lanthanum carbonate recalls
4 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Lanthanum Carbonate chewable tablets, 1000mg* recalled by Cipla USALanthanum Carbonate | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lanthanum Carbonate chewable tablets, 1000mg* recalled by Cipla USALanthanum Carbonate | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lanthanum Carbonate Chewable Tablets, 1000mg recalled by Cipla USA | Cipla USA | Other | Nationwide |
| Drug | CLASS II | Lanthanum Carbonate Chewable Tablets, 1000mg recalled by Cipla USA | Cipla USA | Other | Nationwide |
All lanthanum carbonate recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Lanthanum Carbonate chewable tablets, 1000mg* recalled by Cipla USALanthanum Carbonate | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lanthanum Carbonate chewable tablets, 1000mg* recalled by Cipla USALanthanum Carbonate | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lanthanum Carbonate Chewable Tablets, 1000mg recalled by Cipla USA | Cipla USA | Other | Nationwide |
| Drug | CLASS II | Lanthanum Carbonate Chewable Tablets, 1000mg recalled by Cipla USA | Cipla USA | Other | Nationwide |
Should you stop taking Lanthanum Carbonate?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.