Grx Hicort 25 (hydrocortisone ) Suppositories recalls
The FDA has published 1 recall involving Grx Hicort 25 (hydrocortisone ) Suppositories since 2015. The latest was reported on 9 Dec 2015. Most were for labeling errors. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls1since 2015
Last 12 months0reported
Class I00% of total
Ongoing0latest 9 Dec 2015
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why grx hicort 25 (hydrocortisone ) suppositories is recalled
Companies
By year
All grx hicort 25 (hydrocortisone ) suppositories recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories recalled | Geritrex | Labeling Errors | Nationwide |
Should you stop taking Grx Hicort 25 (hydrocortisone ) Suppositories?
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.