Unomedical S.r.o.
FDA adverse event reports naming Unomedical S.r.o. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: UNOMEDICAL S.R.O..
- Total reports
- 2,735
- Deaths
- 0
- Injuries
- 200
- Malfunctions
- 2,535
Reports per year
211
212
1113
6014
13015
1716
2018
15519
13620
18721
7622
19823
57224
66325
50526
Source: FDA adverse event reports by year received, 2011–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, UrologicalKOD1,264
- Catheter, UrethralGBM1,098
- Tape And Bandage, AdhesiveKGX137
- Pouch, ColostomyEZQ105
- Tube, FeedingFPD47
- Catheters, Suction, TracheobronchialBSY18
- Catheter, Nasal, OxygenBZB10
- Catheter, StraightEZD9
- Urinary Drainage Collection Kit, For Indwelling CatheterFCN8
- Connector, CatheterGCD8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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