Ventilator, emergency, manual (resuscitator)
FDA product code BTM · Class 2 · 311 devices · 101 reports · 3 deaths reported · 274 devices named in recalls
- Portex 8500Icu Medical, Inc. · Ventilator, emergency, manual (resuscitator)1 report
- Portex 8503Icu Medical, Inc. · Ventilator, emergency, manual (resuscitator)1 report
- Portex 8501Icu Medical, Inc. · Ventilator, emergency, manual (resuscitator)1 report
- AirLife 2K7000Carefusion Corporation · Ventilator, Emergency, Manual (Resuscitator)1 report
- Vital Signs 5102RVWCarefusion Corporation · Ventilator, emergency, manual (resuscitator)1 report
- Ventlab AF5000MBVentlab, LLC · Ventilator, Emergency, Manual (Resuscitator)1 report
- Ventlab AF5040MBVentlab, LLC · Ventilator, Emergency, Manual (Resuscitator)1 report
- Ventlab AF3040MBVentlab, LLC · Ventilator, Emergency, Manual (Resuscitator)1 report
- HUDSON RCI IPN039348Teleflex Incorporated · Ventilator, emergency, manual (resuscitator)1 report
- Portex 8503FIcu Medical, Inc. · Ventilator, emergency, manual (resuscitator)1 report
- Portex 8520BMPIcu Medical, Inc. · Ventilator, emergency, manual (resuscitator)1 report