Skip to main content

Embecta Penel Limited - DUN Laoghaire, Ireland

FDA adverse event reports naming Embecta Penel Limited - DUN Laoghaire, Ireland as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND.

Total reports
1,324
Deaths
0
Injuries
34
Malfunctions
1,290

Reports per year

24
25
26

Source: FDA adverse event reports by year received, 20242026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.

Top device categories

Recent recalls

No recalls listed in the FDA device recall database for this entry.

Monitor Embecta Penel Limited - DUN Laoghaire, Ireland automatically

DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.