Eosera recalls
Eosera has 4 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 19 Aug 2020. The most frequent reason is manufacturing (cgmp) deviations.
Total recalls4since 2020
Last 12 months0reported
Class I00% of total
Ongoing0latest 19 Aug 2020
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 100%Class III 0 0%
Why eosera is recalled
Product types
By year
All eosera recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Ear Pain MD Pain Relief Drops For Kids recalled by Eosera | Eosera | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Ear Pain MD Pain Relief Drops with 4% Lidocaine recalled by Eosera | Eosera | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Day & Night Pack Ear Itch MD Anti-Itch Spray recalled by Eosera | Eosera | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%), Eosera recalled | Eosera | Manufacturing (CGMP) Deviations | 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.