Carvediol recalls

The FDA has published 4 recalls involving Carvediol since 2016. The latest was reported on 28 Sep 2016. Most were for potency & assay. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls4since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 28 Sep 2016

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 0 0%Class III 4 100%

Why carvediol is recalled

Potency & Assay4100%

Companies

Sun Pharmaceutical Industries4100%

By year

20164100%

All carvediol recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
28 Sep 2016Drug	CLASS III	Carvediol Tablets, USP, 25 mg bottle recalled	Sun Pharmaceutical Industries	Potency & Assay	Nationwide
28 Sep 2016Drug	CLASS III	Carvediol Tablets, USP, 5 mg bottle recalled	Sun Pharmaceutical Industries	Potency & Assay	Nationwide
28 Sep 2016Drug	CLASS III	Carvediol Tablets, USP, 25 mg bottle recalled	Sun Pharmaceutical Industries	Potency & Assay	Nationwide
28 Sep 2016Drug	CLASS III	Carvediol Tablets , USP, 125 mg bottle recalled	Sun Pharmaceutical Industries	Potency & Assay	Nationwide

Should you stop taking Carvediol?

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.