Oxcarbazepine recalls
The FDA has published 9 recalls involving Oxcarbazepine since 2013. The latest was reported on 7 Jun 2023. Most were for potency & assay. 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 recalls9since 2013
Last 12 months0reported
Class I111% of total
Ongoing1latest 7 Jun 2023
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 11%Class II 7 78%Class III 1 11%
Why oxcarbazepine is recalled
Companies
By year
Ongoing oxcarbazepine recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Oxcarbazepine Oral Suspension, USP, 300 mg recalled by Akorn | Akorn | Potency & Assay | Nationwide |
All oxcarbazepine recalls, newest first
9 totalShould you stop taking Oxcarbazepine?
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.