Bevadex (bevacizumab) Prefilled recalls

The FDA has published 1 recall involving Bevadex (bevacizumab) Prefilled since 2017. The latest was reported on 20 Sep 2017. Most were for sterility. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2017

Last 12 months0reported

Class I00% of total

Ongoing0latest 20 Sep 2017

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 1 100%Class III 0 0%

Why bevadex (bevacizumab) prefilled is recalled

Sterility1100%

Companies

Bella Pharmaceuticals1100%

By year

20171100%

All bevadex (bevacizumab) prefilled recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
20 Sep 2017Drug	CLASS II	BevaDex (bevacizumab) Prefilled (1.25mg/1mg) Syringes recalled	Bella Pharmaceuticals	Sterility	Nationwide

Should you stop taking Bevadex (bevacizumab) Prefilled?

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.