Sulfur recalls
The FDA has published 2 recalls involving Sulfur since 2017. The latest was reported on 24 Feb 2021. Most were for sterility. DLC Laboratories 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 recalls2since 2017
Last 12 months0reported
Class I00% of total
Ongoing0latest 24 Feb 2021
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why sulfur is recalled
Companies
By year
All sulfur recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Sulfur Ointment 10%, Pomada de Azufre recalled by DLC Laboratories | DLC Laboratories | Packaging Defects | Nationwide |
| Drug | CLASS II | Sulfur 5% Cream recalled by Synergy Rx | Synergy Rx | Sterility | Nationwide |
Should you stop taking Sulfur?
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.