Amantadine recalls
The FDA has published 6 recalls involving Amantadine since 2017. The latest was reported on 4 Mar 2026. Most were for potency & assay. AvKARE 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 recalls6since 2017
Last 12 months1reported
Class I00% of total
Ongoing2latest 4 Mar 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 6 100%Class III 0 0%
Why amantadine is recalled
Companies
Brands
By year
Ongoing amantadine recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Amantadine HCl, Capsules, UPS, 100 mg dose recalled by AvKAREAmantadine Hcl | AvKARE | Potency & Assay | Nationwide |
| Drug | CLASS II | Amantadine Hydrochloride Oral Solution USP, 50mg recalled by Akorn | Akorn | Potency & Assay | Nationwide |
All amantadine recalls, newest first
6 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Amantadine HCl, Capsules, UPS, 100 mg dose recalled by AvKAREAmantadine Hcl | AvKARE | Potency & Assay | Nationwide |
| Drug | CLASS II | Amantadine Hydrochloride Oral Solution USP, 50mg recalled by Akorn | Akorn | Potency & Assay | Nationwide |
| Drug | CLASS II | Amantadine Hydrochloride Tablets 100 mg recalled by Cardinal HealthAmantadine Hydrochloride | Cardinal Health | Manufacturing (CGMP) Deviations | FL, GA, SC |
| Drug | CLASS II | Amantadine Hydrochloride Tablets, 100 mg recalled by Jubilant Cadista | Jubilant Cadista Pharmaceuticals | Foreign Material | Nationwide |
| Drug | CLASS II | Amantadine HCl Capsules, USP, 100 mg Unite Dose recalled by AVKAREAmantadine Hcl | AVKARE | Potency & Assay | Nationwide |
| Drug | CLASS II | Amantadine HCl Capsules, USP, 100 mg recalled by Apace KY | Apace KY | Other | KY |
Should you stop taking Amantadine?
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.