| Model Number |
HEM1 |
| Medical Device Problem Code |
Incorrect, Inadequate or Imprecise Result or Readings (1535)
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| Health Effect - Clinical Code |
No Clinical Signs, Symptoms or Conditions (4582)
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| Date of Event |
02/19/2025
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Type of Reportable Event
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Malfunction
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Additional Manufacturer Narrative
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The device evaluation is anticipated.However, the complaint cannot be confirmed without the completion of a product evaluation.A supplemental report will be forthcoming when the investigation is completed.Complaint histories for all reported events are reviewed against trending control limits on a monthly basis and any excursions above the control limits are assessed and documented as a part of the monthly review.Additional fda product code: dqe, qaq, mud, dxn, dsb, qms, fll.
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Event or Problem Description
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It was reported that during use, a hemosphere monitor displayed inaccurate pressure values.The cable and swan ganz module were exchanged, but the issue continued.The issue was resolved by exchanged the monitor.There were no patient injuries.The device is available for evaluation.
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Additional Manufacturer Narrative
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A product evaluation was completed on the returned monitor.The reported event was unable to be confirmed.Monitor displayed normal blood pressure readings and waveform while connected to a known working hemcsm10, hempc2k, hrs and simulator.There were no visible physical damage and no error messages observed.An engineering evaluation was initiated to assess for any manufacturing related processes which could be correlated to the complaint.The reported issue could not be confirmed with product evaluation and no product nor process malfunction was identified.A device history record review was completed and documented that device met all specifications upon distribution.The hemosphere operator's manual states that causes of blood temperature variations include, but are not limited to: status post cardiopulmonary bypass surgery, centrally administered cooled or warmed solutions of blood products, and use of sequential compression devices.
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Search Alerts/Recalls
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