Model 3300 LATITUDE Programming System with installed Model 3892 ALTRUA, INSIGNIA I, NEXUS I Software Support Application
FDA Recall Z-0319-2021 · Posted None
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Recalling FirmBoston Scientific Corporation
Recall StatusTerminated
Product CodeLWS
Date Initiated2020-09-22
Date Terminated2024-09-04
Product Quantity8 devices
Reason for Recall
There is potential when a user changes an EGM trace channel with a Manual Pace Threshold test in progress that the newly modified trace channel may change to a flat line.
Firm Action
Boston Scientific sales representatives will hand-deliver a removal letter to all customer consignees with one of the eight affected Model 3300 LATITUDE programmer. BSC sales representatives will maintain control of these devices.
In order to continue to provide the benefits that this software support application
provides for those patients implanted with an ALTRUA/INSIGNIA I pacemaker,
BSC sales representatives will continue to use Model 3300 LATITUDE programmers
installed with the Model 3892 v1.04 ALTRUA / INSIGNIA I / NEXUS I Software
Support Application in the field. The risks associated with this unintended behavior
can be avoided when specific remedial actions are adhered to. These remedial actions will be adhered to until a software correction is approved and installed on these programmers.
BSC will confirm via email from sales representatives that 100% of the removal
letters were delivered.
BSC will post the removal letter on the BSC website within the Product Performance Resource Center located @ www.bostonscientific.com/en-US/pprc/productadvisories.html.
Root Cause
Software design
Distribution Pattern
Distributed in US - AR, FL, IL, and TX
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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