Midodrine recalls

The FDA has published 2 recalls involving Midodrine since 2014. The latest was reported on 11 Mar 2026. Most were for labeling errors. The Harvard Drug Group 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 recalls2since 2014

Last 12 months1reported

Class I00% of total

Ongoing1latest 11 Mar 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 1 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 2 100%Class III 0 0%

Why midodrine is recalled

Labeling Errors150%
Packaging Defects150%

Companies

The Harvard Drug Group150%
Aidapak Services150%

By year

2026150%
2014150%

Ongoing midodrine recalls

1 active

Reported	Class	Recall	Company	Reason	Where
11 Mar 2026Drug	CLASS II	Midodrine Hydrochloride Tablets, USP, 5 mg ( blister packs) recalledMidodrine Hydrochloride	The Harvard Drug Group	Packaging Defects	Nationwide

All midodrine recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
11 Mar 2026Drug	CLASS II	Midodrine Hydrochloride Tablets, USP, 5 mg ( blister packs) recalledMidodrine Hydrochloride	The Harvard Drug Group	Packaging Defects	Nationwide
29 Jan 2014Drug	CLASS II	Midodrine HCL, Tablet, 2.5 mg recalled by Aidapak Services	Aidapak Services	Labeling Errors	4 states

Should you stop taking Midodrine?

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.