Zoledronic Acid Per recalls

The FDA has published 1 recall involving Zoledronic Acid Per since 2014. The latest was reported on 8 Oct 2014. 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 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 8 Oct 2014

Recalls per month, last 24 months

click a bar for that month

0Dec '24 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0 0Dec 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0

Severity split

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

Why zoledronic acid per is recalled

Sterility1100%

Companies

Sagent Pharmaceuticals1100%

By year

20141100%

All zoledronic acid per recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
8 Oct 2014Drug	CLASS II	Zoledronic Acid Injection 5 mg per (0.05 mg/mL) single-use recalled	Sagent Pharmaceuticals	Sterility	Nationwide

Should you stop taking Zoledronic Acid Per?

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.