Monitor, Breathing Frequency
FDA adverse event reports and recall history for monitor, breathing frequency (product code BZQ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 127
- Deaths
- 11
- Injuries
- 13
- Malfunctions
- 95
Reports per year
Source: FDA adverse event reports by year received, 2003–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2011-02-03TerminatedEmployee error
ThermiSense model 5700-A5 The ThermiSense Model 5700-A5 is a nasal cannula that detects thermal variation during breathing cycles and transmits those variations to a remote Alice-5 Polysomnograph via electrical connectors to monitors an adult patient's breathing rate in a sleep laboratory study
The incorrect length and connector were utilized in lot 110810 of the ThermiSense Alice 5, making the product unusable as it will not interface with the sleep labs equipment.
- 2004-07-27TerminatedOther
Battery Pack Respironics Model 915 for use in the 900 Series SmartMonitor and the 900 Series Pulse Oximeter.
Recalling firm received a product complaint from a customer that the lead wire from Model 915 battery was not connected.
- 2004-07-20TerminatedOther
Model 511 Cardio Respiratory Monitor with Oximax technology with software version 5.0
Device may not alarm for %SpO2 value limit violations if a specific feature is enabled
Monitor monitor, breathing frequency automatically
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