Puritan Bennett Corp.
FDA adverse event reports naming Puritan Bennett Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: PURITAN BENNETT CORP..
- Total reports
- 1,121
- Deaths
- 22
- Injuries
- 37
- Malfunctions
- 1,051
Reports per year
2097
1798
499
300
401
402
303
204
905
1606
4707
5008
33209
40810
16511
Source: FDA adverse event reports by year received, 1997–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Ventilator, Continuous, Facility UseCBK1,097
- Generator, Oxygen, PortableCAW9
- Unit, Liquid-Oxygen, PortableBYJ7
- Ventilator, Emergency, Manual (Resuscitator)BTM2
- Product code 1
- Mask, OxygenBYG1
- Ventilator, Non-Continuous (Respirator)BZD1
- Set, Tubing And Support, Ventilator (W Harness)BZO1
- Monitor, Breathing FrequencyBZQ1
- Regulator, Pressure, Gas CylinderCAN1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Puritan Bennett Corp. 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.