Terazosin recalls

The FDA has published 3 recalls involving Terazosin since 2013. The latest was reported on 29 Jan 2014. Most were for packaging defects. Teva Pharmaceuticals USA 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 29 Jan 2014

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 0 0%Class II 3 100%Class III 0 0%

Why terazosin is recalled

Packaging Defects267%
Labeling Errors133%

Companies

Teva Pharmaceuticals USA267%
Aidapak Services133%

By year

2014133%
2013267%

All terazosin recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
29 Jan 2014Drug	CLASS II	Terazosin HCL, Capsule, 5 mg recalled by Aidapak Services	Aidapak Services	Labeling Errors	4 states
14 Aug 2013Drug	CLASS II	Terazosin Hydrochloride Capsules,10 mg recalled	Teva Pharmaceuticals USA	Packaging Defects	Nationwide
20 Mar 2013Drug	CLASS II	Terazosin Hydrochloride Capsules, 2 mg recalled	Teva Pharmaceuticals USA	Packaging Defects	Nationwide

Should you stop taking Terazosin?

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.