Allegiance Healthcare Corp.
FDA adverse event reports naming Allegiance Healthcare Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALLEGIANCE HEALTHCARE CORP..
- Total reports
- 1,209
- Deaths
- 14
- Injuries
- 169
- Malfunctions
- 519
Reports per year
Source: FDA adverse event reports by year received, 1995–2008. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Latex Patient Examination GloveLYY415
- Apparatus, Suction, Single Patient Use, Portable, NonpoweredGCY121
- Instrument, BiopsyKNW100
- Bottle, Collection, VacuumKDQ77
- Ventilator, Emergency, Manual (Resuscitator)BTM43
- Heater, Breathing System W/Wo Controller (Not Humidifier Or NebulizerBZE37
- General Surgery TrayLRO27
- Set, Tubing And Support, Ventilator (W Harness)BZO25
- Pack, Hot Or Cold, DisposableIMD21
- Set, Tubing, Blood, With And Without Anti-Regurgitation ValveFJK20
Recent recalls
- 2003-02-25TerminatedOther
Convertors Three Quarter Sheet (Drape Sheet), catalog #29350; Allegiance Healthcare Corporation, McGaw Park, IL 60085 USA; individually packaged drapes, 20 packages per case
The product labeled as sterile had not been through its sterilzation cycle.
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