CME McKinley

T and T34 Syringe Pumps

T34 Addendum to Instructions for Use Feb 2021

Addendum

4 Pages

1030 Eskdale Road Winnersh Triangle Wokingham RG41 5TS www.BD.com  February 5, 2021  URGENT: FIELD SAFETY NOTICE – MMS-21-3992 T34 TM Ambulatory Syringe Pumps 3rd Editions Serial numbers: All Serial Numbers Type of Action: Advisory Attention: Clinical Engineering Managers, Clinical Personnel, Risk Managers This letter contains important information which requires your attention. Dear Customer, BD is issuing this field safety notice to advise of an update being made to the Directions for Use (DFU) for the 3rd Edition T34™ Ambulatory Syringe Pumps. Our distribution records indicate that your organisation may have received impacted pumps.  Description of the Problem BD has become aware through customer feedback that if the T34™ 3rd Edition Ambulatory Syringe Pump is stored without the main 9V battery for several days or weeks, it may result in partial or full depletion of the 3V internal battery. The 3V battery powers the internal real-time clock. The 3V depletion may trigger two different issues: “Timer’s battery fail” alarm and real-time clock time lag/delay. To address the issue, BD is communicating an update to information in the Directions for Use for the 3 rd Edition T34™ Ambulatory Syringe Pumps (DFU999-103EN Rev. 04). The following 2 statements are to be used in addition to the current DFU contents. Section 1.7 - Syringe Pump and Unpacking Verify that the date and time are accurate before starting the infusion by checking the last entry in the event log. If the date and time are not correct, adjust the date and time per Section 5.6 of the DFU (Practice Scenarios for Changing Pump Configuration). Section 8.3 - Pump Storage If the pump is stored without a 9V battery verify the date and time are accurate before starting the infusion by checking the last entry in the event log. In the case, date and time is not correct, please adjust date and time accordingly. Programming and running an infusion isn´t dependent on a properly set internal Real Time Clock and it will not cause any safety risks for patients if the internal Real Time Clock is not properly set. The clock is not visible from the main screen of the pump, the time lag will be noticed in the Event log only (directly in Events Log option in the pump menu or via BodyComm™). Although the time and date would be incorrect, the sequence and the time between events would be correct. The event log can be impacted by an incorrect internal Real Time Clock. This may have an impact on clinical investigations and audit trails, requiring event log timings, if the Real Time Clock is not correctly set, however, the investigator would still be able to obtain data to assist any investigation. BD has issued the following Technical Service Bulletin (TB08675 Rev. 00) on how to resolve any time lag issues associated with the event described above.  EMEAFA0094 Revision 1  Page 1 of 3
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