Black Ant recalls

The FDA has published 4 recalls involving Black Ant since 2014. The latest was reported on 7 Feb 2018. Most were for labeling errors. A&H Focal 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 months0reported

Class I375% of total

Ongoing0latest 7 Feb 2018

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 0Jul 0 0

Severity split

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

Why black ant is recalled

Labeling Errors375%
Hidden Drug Ingredients125%

Companies

By year

2018125%
2014375%

All black ant recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
7 Feb 2018Drug	CLASS II	Black Ant capsules, 4600mg, labeling is in foreign language recalled	A&H Focal	Hidden Drug Ingredients	NJ, NY
8 Oct 2014Drug	CLASS I	Black Ant, 2800 mg, four capsules recalled by Eugene Oregon	Eugene Oregon	Labeling Errors	11 states
24 Sep 2014Drug	CLASS I	Black Ant, 4600 mg, four capsules recalled by Nova Products	Nova Products	Labeling Errors	Nationwide
16 Apr 2014Drug	CLASS I	Black Ant, 4600 mg x Product recalled by American Lifestyle.Com	American Lifestyle.Com	Labeling Errors	NY

Should you stop taking Black Ant?

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.