Poractant Alfa recalls

The FDA has published 1 recall involving Poractant Alfa since 2026. The latest was reported on 1 Apr 2026. 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 2026

Last 12 months1reported

Class I00% of total

Ongoing1latest 1 Apr 2026

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 1Apr 0 0 0Jul 0 0

Severity split

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

Why poractant alfa is recalled

Sterility1100%

Companies

Chiesi USA1100%

By year

20261100%

Ongoing poractant alfa recalls

1 active

Reported	Class	Recall	Company	Reason	Where
1 Apr 2026Drug	CLASS II	Curosurf (poractant alfa), 240 mg recalled by Chiesi USACurosurf	Chiesi USA	Sterility	Nationwide

All poractant alfa recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
1 Apr 2026Drug	CLASS II	Curosurf (poractant alfa), 240 mg recalled by Chiesi USACurosurf	Chiesi USA	Sterility	Nationwide

Should you stop taking Poractant Alfa?

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.