Lithium Carbonate recalls
The FDA has published 4 recalls involving Lithium Carbonate since 2014. The latest was reported on 3 Jan 2024. Most were for packaging defects. Aidapak Services has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls4since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 3 Jan 2024
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 lithium carbonate is recalled
Companies
By year
All lithium carbonate recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Lithium Carbonate Extended-Release Tablets, USP, 300 mg recalled | Cardinal Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Lithium Carbonate ER, Tablet, 300 mg recalled by Aidapak Services | Aidapak Services | Packaging Defects | 4 states |
| Drug | CLASS II | Lithium Carbonate ER, Tablet, 225 mg (1/2 of 450 mg) recalled | Aidapak Services | Packaging Defects | 4 states |
| Drug | CLASS II | Lithium Carbonate ER, Tablet, 450 mg recalled by Aidapak Services | Aidapak Services | Packaging Defects | 4 states |
Should you stop taking Lithium 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.