Uromedica recalls
Uromedica has 2 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 12 Jan 2022. The most frequent reason is sterility.
Total recalls2since 2020
Last 12 months0reported
Class I00% of total
Ongoing0latest 12 Jan 2022
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 uromedica is recalled
Product types
By year
All uromedica recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Implantation Instrument Set (Sheath and Sharp Trocar) recalled | Uromedica | Sterility | Nationwide |
| Device | CLASS II | ProACT Implantation Instrument Set, is a reusable recalled by Uromedica | Uromedica | Sterility | 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.