Fyremadel recalls
Fyremadel products have been recalled 1 time, most recently on 3 May 2023. The recalling company is usually Sun Pharmaceutical Industries. The most common reason is particulate matter.
Total recalls1since 2023
Last 12 months0reported
Class I00% of total
Ongoing0latest 3 May 2023
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 fyremadel is recalled
Companies
Product types
By year
All fyremadel recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Fyremadel (ganirelix acetate) injection, 250 mcg recalledFyremadel | Sun Pharmaceutical Industries | Particulate Matter | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.