Ifosfamide recalls

The FDA has published 3 recalls involving Ifosfamide since 2013. The latest was reported on 21 Aug 2019. Most were for temperature abuse. AmeriSource Bergen 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 21 Aug 2019

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 3 100%Class III 0 0%

Why ifosfamide is recalled

Temperature Abuse267%
Sterility133%

Companies

AmeriSource Bergen267%
Infusion Options133%

By year

2019133%
2013267%

All ifosfamide recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
21 Aug 2019Drug	CLASS II	Ifosfamide 9200 MG / Ns Ivpb With Mesna 9200 MG recalled	Infusion Options	Sterility	NY
9 Oct 2013Drug	CLASS II	Ifosfamide Injection, Single dose vial recalled by AmeriSource Bergen	AmeriSource Bergen	Temperature Abuse	Nationwide
9 Oct 2013Drug	CLASS II	Ifosfamide Injection, Single dose vial recalled by AmeriSource Bergen	AmeriSource Bergen	Temperature Abuse	Nationwide

Should you stop taking Ifosfamide?

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.