Terumo Advanced Perfusion System 1 Electronic Patient Gas System Catalog #: 801188
FDA Recall Z-2350-2021 · Posted None
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Recalling FirmTerumo Cardiovascular Systems Corporation
Recall StatusTerminated
Product CodeDTQ
Date Initiated2021-06-08
Date Terminated2022-06-28
Product Quantity1 unit OUS
Reason for Recall
intermittent failure causes a blender initialization fault upon start-up, or during an EPGS calibration attempt following the 15-minute warm-up period. The control sliders on the Central Control Monitor (CCM) are disabled and the gas system can only be controlled by the local control knobs
Firm Action
Terumo notified the regional affiliate to address the single EPGS device in Panama via email on 6/8/21. Letter states reason for recall, health risk and action to take:
Terumo CVS will execute a field correction to replace the one (1) affected EPGS device. A Terumo Representative will contact you to schedule the field correction activities.
1. Review this Medical Device Correction and assure the user has received notice of this issue.
2. A Terumo representative will contact the user to schedule the field correction activity.
Note: Terumo CVS recommends that users continue using the affected Terumo System 1 while waiting for this correction.
We encourage you to contact your local Terumo representative with any questions or concerns.
Root Cause
Nonconforming Material/Component
Distribution Pattern
International distribution in the country of Panama.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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