Cyproheptadine recalls

The FDA has published 4 recalls involving Cyproheptadine since 2014. The latest was reported on 29 Jul 2026. Most were for labeling errors. Lyne Laboratories 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 months1reported

Class I00% of total

Ongoing1latest 29 Jul 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 0 0Apr 0 0 1Jul 0 0

Severity split

Class I 0 0%Class II 3 75%Class III 1 25%

Why cyproheptadine is recalled

Companies

By year

2026125%
2019125%
2016125%
2014125%

Ongoing cyproheptadine recalls

1 active

Reported	Class	Recall	Company	Reason	Where
29 Jul 2026Drug	CLASS II	Rising, Cyproheptadine Hydrochloride Syrup, 2mg recalledCyproheptadine Hydrochloride	Rising Pharma Holding	Particulate Matter	Nationwide

All cyproheptadine recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
29 Jul 2026Drug	CLASS II	Rising, Cyproheptadine Hydrochloride Syrup, 2mg recalledCyproheptadine Hydrochloride	Rising Pharma Holding	Particulate Matter	Nationwide
19 Jun 2019Drug	CLASS II	Cyproheptadine Hydrochloride Syrup Oral Solution, USP, 2mg recalled	Torrent Pharma	Sterility	Nationwide
13 Jul 2016Drug	CLASS III	Cyproheptadine Hydrochloride Syrup, Oral Solution USP, 2 mg recalled	Lyne Laboratories	Potency & Assay	NJ
22 Jan 2014Drug	CLASS II	Cyproheptadine HCL Tablet, 4 mg recalled by Aidapak Services	Aidapak Services	Labeling Errors	4 states

Should you stop taking Cyproheptadine?

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.