Arjohuntleigh Polska SP. Z O.O.
FDA adverse event reports naming Arjohuntleigh Polska SP. Z O.O. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ARJOHUNTLEIGH POLSKA SP. Z O.O..
- Total reports
- 1,887
- Deaths
- 38
- Injuries
- 466
- Malfunctions
- 1,374
Reports per year
1112
1613
2514
4215
8516
6917
2418
3219
15920
16021
21922
29723
32524
31525
10826
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Bed, Ac-Powered Adjustable HospitalFNL1,231
- Lift, Patient, Non-Ac-PoweredFSA354
- Mattress, Air Flotation, Alternating PressureFNM78
- Mattress, Flotation Therapy, Non-PoweredIKY61
- Bath, Hydro-MassageILJ61
- Sleeve, Limb, CompressibleJOW29
- Bed, Flotation Therapy, PoweredIOQ17
- Washer Of Body Waste ReceptaclesFLH13
- Bath, Sitz, PoweredILM13
- Aid, TransferIKX11
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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