Solu-cortef (hydrocortisone recalls

The FDA has published 1 recall involving Solu-cortef (hydrocortisone since 2016. The latest was reported on 3 Feb 2016. 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 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 3 Feb 2016

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 1 100%Class III 0 0%

Why solu-cortef (hydrocortisone is recalled

Sterility1100%

Companies

Sentara Enterprises1100%

By year

20161100%

All solu-cortef (hydrocortisone recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
3 Feb 2016Drug	CLASS II	Solu-Cortef (hydrocortisone) 1MG in NS recalled by Sentara Enterprises	Sentara Enterprises	Sterility	NC, VA

Should you stop taking Solu-cortef (hydrocortisone?

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.