Zimmer ATS 3000
Zimmer · Model ATS 3000
Innovative Limb Occlusion Pressure(LOP) feature. Uses ambient air. Uses electronic and microprocessor regulated pressure. Self-Check Calibration automatically checks the accuracy of the machine calibration each time the unit is powered on. Cuff Alert alerts the user of cuff status when an attempt is made to set the machine on standby. Cuff Lockout feature prompts the user to confirm the deflation command during bilateral or IVRA procedure in order to reduce complications due to sudden cuff deflation of the second cuff.
Error Codes
Extracted directly from this unit's own service manual.
E003SYSTEM FAIL A pneumatic system error was detected during self-test. Cycle the ON/STANDBY button. If problem persists, note error code and contact manufacturer.
E004WDT FAIL A Safety Monitor timing error was detected. Cycle the ON/ STANDBY button. If problem persists, note error code and contact manufacturer.
E005VALVE FAIL The Safety Monitor detected an illegal valve state. Cycle the ON/ STANDBY button. If problem persists, note error code and contact manufacturer.
E006SYSTEM FAIL A Safety Monitor detection error was detected. Cycle the ON/ STANDBY button. If problem persists, note error code and contact manufacturer. A.T.S.
E008SYSTEM FAIL The processor received an unknown interrupt. Cycle the ON/STANDBY button. If problem persists, note error code and contact manufacturer.
E010ROM FAIL A non-volatile memory value was detected during power-up. Cycle the ON/STANDBY button. If problem persists, note error code and contact manufacturer.
E011ROM FAIL ROM check error detected a self-test. Cycle the ON/STANDBY button. If problem persists, note error code and contact manufacturer.
E012RAM FAIL A microprocessor RAM error was detected during self-test. Cycle the ON/STANDBY button. If problem persists, note error code and contact manufacturer.
E013BATTERY FAIL Battery voltage below minimum threshold. Plug unit in and cycle the ON/STANDBY button. If problem persists, note error code and contact manufacturer.
E014BATTERY FAIL A battery charging circuit failure was detected at power-up. Verify a battery is connected and cycle the ON/STANDBY button. If problem persists, note error code and contact manufacturer.
E015CAL FAIL Incorrect zero pressure calibration point was detected. Calibrate unit. If problem persists, note error code and contact manufacturer.
E016CAL FAIL Incorrect calibration point was detected. Calibrate unit. If problem persists, note error code and contact manufacturer.
E017CAL FAIL Calibration error was detected. Calibrate unit. If problem persists, note error code and contact manufacturer.
E018CAL M FAIL Main cuff transducer calibration error was detected. Calibrate unit. If problem persists, note error code and contact manufacturer.
E019CAL 2 FAIL Second cuff transducer calibration error was detected. Calibrate unit. If problem persists, note error code and contact manufacturer.
Documents & Manuals
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000 tourniquets after receiving complaints of both out-of-box failures and failures during surgical procedures on some of the affected units. During failure the unit will alarm, lock into a non-operational mode, and the display screen will go blank. Based on investigation, this problem appears to be due to a counterfeit chip on the
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