Fisher & Paykel Healthcare Limited
FDA adverse event reports naming Fisher & Paykel Healthcare Limited as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: FISHER & PAYKEL HEALTHCARE LIMITED.
- Total reports
- 2,192
- Deaths
- 6
- Injuries
- 30
- Malfunctions
- 2,139
Reports per year
23812
40113
29214
10415
10716
12017
8618
9219
1920
3721
10122
6723
1624
1825
726
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
- Humidifier, Respiratory Gas, (Direct Patient Interface)BTT989
- Heater, Breathing System W/Wo Controller (Not Humidifier Or NebulizerBZE527
- Warmer, Infant RadiantFMT200
- Ventilator, Emergency, Powered (Resuscitator)BTL172
- Set, Tubing And Support, Ventilator (W Harness)BZO141
- Cannula, Nasal, OxygenCAT79
- Ventilator, Non-Continuous (Respirator)BZD40
- Sv70 VentilatorMNT25
- Mask, OxygenBYG10
- Connector, Airway (Extension)BZA3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Fisher & Paykel Healthcare Limited 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.