
Zimmer · Model Inflatomatic 3000
Tourniquet Zimmer Inflatomatic.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Pressure droops during a case, will not inflate to setpoint, leak alarm.
Root cause: Internal pump / compressor wear, a solenoid-valve fault, or a leak in the tubing / cuff / connectors.
Symptoms: Displayed pressure differs from an independent gauge - patient-safety critical.
Root cause: Pressure-transducer drift or a calibration fault.
Symptoms: One channel will not regulate independently, cross-talk between channels.
Root cause: Channel solenoid / transducer or a manifold fault.
Symptoms: Inflation-time alarm not sounding, timer wrong.
Root cause: Alarm / timer board fault - a safety function.
Symptoms: Leak at the connector, cuff will not hold.
Root cause: Worn tubing, connectors, or a damaged cuff.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
Verify against a calibrated gauge after replacement.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Internal pump / compressor | Major service part | $$$ | Difficult |
| Solenoid / regulator valve | Major service part | $$ | Moderate |
| Pressure transducer Verify against a calibrated gauge after replacement. | Periodic replacement | $$ | Moderate |
| Connecting tubing / connectors | Frequent wear item | $ | Easy |
| Alarm / control board | Major service part | $$ | Moderate |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
No documents available for this device yet.
Synced live from the FDA openFDA API.
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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