Pyridostigmine recalls
The FDA has published 3 recalls involving Pyridostigmine since 2013. The latest was reported on 2 Nov 2022. Most were for potency & assay. Corepharma 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 recalls3since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 2 Nov 2022
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why pyridostigmine is recalled
Companies
By year
All pyridostigmine recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Pyridostigmine Bromide Oral Solution, USP 60 mg/ Delivers recalledPyridostigmine Bromide | VistaPharm | Potency & Assay | Nationwide |
| Drug | CLASS II | Pyridostigmine Bromide Tablets USP, 60 mg recalled by Corepharma | Corepharma | Potency & Assay | Nationwide |
| Drug | CLASS II | Pyridostigmine Bromide Tablets 60 mg recalled by Core Pharma | Core Pharma | Potency & Assay | Nationwide |
Should you stop taking Pyridostigmine?
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.