Every recall we track for Oridion Medical 1987 Ltd. — 47 in all — plus the complaints and injury reports the public filed about them.
Oridion Medical recalls Microstream CO2 filter lines for adult-pediatric use due to risk of treatment delay or unintended extubation during procedures like suctioning, potentially causing respiratory failure.
Oridion Medical recalls Microstream infant CO2 sampling lines due to risk of treatment delay during suctioning. Affected units may cause unintended extubation, respiratory failure, or hypoxia.
Oridion Medical recalls Microstream CO2 sampling lines for neonatal and adult patients due to risk of treatment delay and respiratory failure if adapter cannot be disconnected during procedures like suctioning.
Oridion Medical recalls OmniVentLine Set CO2 sampling lines due to risk of treatment delays and unintended extubation during suctioning procedures.
Oridion Medical recalls Microstream CO2 sampling lines for adults and pediatrics. Users may have trouble disconnecting the adapter from endotracheal tubes during suctioning, risking treatment delays or unintended extubation. This recall affects specific model numbers and serial numbers listed in the notice.
Oridion Medical recalls Microstream airway adapters and CO2 sampling lines that may cause treatment delays or unintended extubation during suctioning, risking respiratory failure. Affected units include specific part numbers and revisions.
Oridion Medical recalls certain Microstream CO2 sampling lines and airway adapters for neonatal and adult/pediatric use. These devices may cause treatment delays or unintended extubation during suctioning procedures, risking respiratory failure or hypoxia.
Oridion Medical recalls certain Microstream CO2 filter lines for neonatal and infant intubation. These lines may cause difficulty disconnecting during suctioning, risking treatment delays or unintended extubation.
Oridion Medical recalls adult and pediatric intubated filter lines that may cause treatment delays or unintended extubation during suctioning procedures, risking respiratory failure.
Oridion Medical recalls CAPNOSTREAM 20 (US) N patient monitors with part numbers CS08651 and others due to potential reset of date/time, nurse call, and alarm settings when powered off. Affected units may need verification.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors with part numbers CS08651-02 and B836141101-B836141120 (and others) due to date/time and alarm settings resetting to factory defaults when powered off.
Oridion Medical recalls Capnostream20 bedside monitors with part number CS08659 that reset date/time and alarm settings when powered off. Affected units may require reconfiguration to prevent incorrect patient monitoring.
Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory settings when powered off. This could affect patient monitoring accuracy. Affected units have specific serial numbers listed in the recall.
Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory settings when powered off. This could affect patient monitoring accuracy. Contact Oridion for details.
Oridion Medical recalls CAPNOSTREAM 20P patient monitors that may reset to factory defaults when powered off. This could affect alarm and nurse call settings.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory settings when powered off. Affected units have specific model numbers and serial ranges. No immediate action is required but users should verify settings.
Oridion Medical recalls CAPNOSTREAM 20P patient monitors that may reset to factory default settings when powered off. Affected units have specific part numbers listed in the recall notice. No immediate action is required but users should check their device settings.
Oridion Medical recalls Capnostream20 N W/PRINTER models with resettable alarm settings. Users may need to adjust settings after power-off to avoid incorrect patient monitoring.
Oridion Medical recalls certain Capnostream20 bedside monitors that may reset to factory defaults when powered off. This could affect patient monitoring settings.
Oridion Medical recalls CAPNOSTREAM 20P bedside patient monitors that may reset date/time, nurse call, and alarm settings to factory defaults when powered off. This could affect patient monitoring safety.
Oridion's CAPNOSTREAM 20P bedside monitors may reset to factory settings when powered off. Affected units have specific part numbers listed in the recall. No action needed if settings remain correct.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that reset to factory settings when powered off. This may affect patient monitoring accuracy.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset date/time and alarm settings to factory defaults when powered off. Affected units have specific part numbers listed in the recall notice.
Oridion Medical recalls Capnostream20 bedside monitors with part numbers CS08751 and others that may reset date/time and alarm settings to factory defaults when powered off. This could affect patient monitoring accuracy.
Oridion Medical recalls certain Capnostream20 bedside monitors that may reset to factory settings when powered off. Affected units include specific model numbers and serial ranges.
Oridion Medical recalls certain Capnostream20 bedside monitors that may reset to factory defaults when powered off. Affected units include specific model numbers and refurbishment codes.
Oridion Medical recalls Capnostream20 monitors (part CS08750) due to potential resetting of alarm settings when powered off. Affected units may require reconfiguration to prevent safety risks.
Oridion Medical recalls refurbished Capnostream20 bedside monitors that may reset to factory settings when powered off. This could affect patient monitoring accuracy. Affected units have specific part numbers.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory settings when powered off. Affected units have specific part numbers. No remedy provided in recall notice.
Oridion Medical recalls certain Capnostream20 N CYVITAL bedside monitors that may reset to factory settings when powered off. Affected units include specific model numbers listed in the recall notice.
Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory settings when powered off. This could affect alarm and nurse call functions. Affected units have specific part numbers listed in the recall.
Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory settings when powered off. This could affect patient monitoring accuracy. Affected units have specific serial numbers.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory settings when powered off, potentially affecting patient safety settings.
Oridion Medical recalls CAPNOSTREAM 20 bedside monitors with part number CS08657 that reset date/time and alarm settings when powered off. Affected units may have incorrect settings after power cycles.
Oridion Medical recalls Capnostream20 M monitors with part number CS08653 and specific serial numbers due to potential reset of date/time and alarm settings when powered off, which could affect patient monitoring accuracy.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory defaults when powered off, potentially causing incorrect patient monitoring settings.
Oridion Medical recalls CAPNOSTREAM 20 bedside monitors that may reset to factory defaults when powered off. Affected units have specific part numbers. No remedy is stated in the recall notice.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory defaults when powered off. Affected units have specific part numbers. No immediate action needed as settings reset is not a safety hazard.
Oridion Medical recalls Capnostream20 M NICU monitors (CS08654RN) that reset alarm settings when powered off. Affected units may require reconfiguration to avoid incorrect patient monitoring.
Orid: Capnostream20 bedside monitors may reset to factory defaults when powered off. Affected units include specific model numbers and refurbished versions.
Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory defaults when powered off, potentially causing alarm settings to malfunction. Affected units include specific model numbers listed in the recall notice.
Oridion Medical recalls CAPNOSTREAM 20 bedside monitors that may reset to factory settings when powered off, potentially causing incorrect patient monitoring.
Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory defaults when powered off, potentially affecting patient safety settings.
Oridion Medical recalls CAPNOSTREAM 20P patient monitors that may reset date/time and alarm settings to factory defaults when powered off. No immediate action needed but check settings.
Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory defaults when powered off. Affected units have specific serial numbers. No immediate action needed but check settings after power cycles.
Oridion Medical recalls Capnostream20 M adult ICU monitors (CS08654RA) due to potential reset of alarm settings when powered off. Affected units may require reconfiguration.
