Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse Generator Models 6660, 6661, 6662, 6663
FDA Recall Z-0023-2018 · Posted None
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Recalling FirmSt. Jude Medical, Inc.
Recall StatusTerminated
Product CodeMHY
Date Initiated2017-09-12
Date Terminated2020-04-16
Product Quantity3,119 devices
Reason for Recall
Analysis of the difference between the actual device longevity and the battery indicator status provided by the Clinician Programmer (CP) or Patient Controller (PC) has revealed errors in the CP or PC longevity estimations that can overestimate or under estimate the battery indicator status in certain situations.
Firm Action
St. Jude Medical sent an Important Medical Device Advisory letter dated September 12, 2017, to all affected customers. Customers were advised the following:
Phase I: ERI Assessment
If a patient reports that an ERI message is displayed on the PC, please contact your Abbott
Representative to obtain the device-specific generator logs and to conduct the ERI Assessment using the
steps in Appendix B prior to making an elective replacement decision.
After the ERI Assessment is completed, follow-up communication from your Abbott representative will
be provided in order to make appropriate decisions. The response will be one of two possible responses:
o ERI is valid at this time for this device, follow existing information provided by IFU and CP for
the elective replacement window for this device.
o The device has the appropriate level of battery voltage to provide the existing therapy until the
next assessment, which should occur no later than March 2018. During this period, the ERI
message will be displayed on the PC at the start of each session. This message may be
dismissed to enter the session on the PC.
Phase II: ERI Software Update
Abbott will deploy a software upgrade, upon approval by local governing agencies that addresses the errors in
calculation causing the inappropriate ERI message. When this software update is deployed, the Phase I ERI
assessment process is no longer needed. After the CP is updated, replacement decisions can be made following
the revised instructions for use, which will be available at manuals.sjm.com. Once approved for use in your
area, notification of the availability of this software update will occur through the Apple Public App Store for
the PC and through the SJM App Catalog for the CP.
Should you have questions about patient management, including questions regarding error messages related to
IPGs, please contact your local Sales Representative or Abbott Support at 1-800-727-7846 (Opt3) (U.S) and
+46 8 474 414
Root Cause
Software design
Distribution Pattern
Worldwide Distribution - US (nationwide) (foreign consignee list will be provide by the firm at a later time)
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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