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
- 1,901
- Deaths
- 38
- Injuries
- 468
- Malfunctions
- 1,386
Reports per year
1112
1613
2514
4215
8516
6917
2418
3219
15920
16021
21922
29723
32524
31525
12226
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Bed, Ac-Powered Adjustable HospitalFNL1,241
- Lift, Patient, Non-Ac-PoweredFSA358
- 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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