Perindopril Erbumine recalls

The FDA has published 1 recall involving Perindopril Erbumine since 2013. The latest was reported on 23 Jan 2013. 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 recalls1since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 23 Jan 2013

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 0 0%Class III 1 100%

Why perindopril erbumine is recalled

Potency & Assay1100%

Companies

Boehringer Ingelheim Roxane1100%

By year

20131100%

All perindopril erbumine recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
23 Jan 2013Drug	CLASS III	Perindopril Erbumine Tablets, 8mg recalled	Boehringer Ingelheim Roxane	Potency & Assay	Nationwide

Should you stop taking Perindopril Erbumine?

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.