Reported Oct 25, 2017 · Terminated

Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse Generator Models 6660, 6661, 6662, 6663

St. Jude Medical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: St. Jude Medical, Inc. · 6901 Preston Rd · Plano, TX · 75024-2508

Is this the product you have?

  • Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse Generator Models 6660, 6661, 6662, 6663
Lot codes and dates
  • Serials implanted prior to September 12, 2017 are considered part of this advisory; Serial Numbers -

    3,119 of 3,119 codes

    • AAD193.1
    • AAD194.1
    • AAD213.1
    • AAD255.1
    • AAD257.1
    • AAD261.1
    • AAD276.1
    • AAD279.1
    • AAD281.1
    • AAD298.1
    • AAD299.1
    • AAD302.1
    • AAD309.1
    • AAD328.1
    • AAD372.1
    • AAD376.1
    • AAD380.1
    • AAN940.1
    • AAN946.1
    • AAN951.1
    • AAN977.1
    • AAN997.1
    • AAP006.1
    • AAP007.1
    • AAP030.1
    • AAP035.1
    • AAP108.1
    • AAP132.1
    • AAP140.1
    • AAP149.1
    • AAP193.1
    • AAP217.1
    • AAP266.1
    • AAP273.1
    • AAP279.1
    • AAP293.1
    • AAP314.1
    • AAP328.1
    • AAP333.1
    • AAP362.1
    • AAP363.1
    • AAP375.1
    • AAP376.1
    • AAP385.1
    • AAP387.1
    • AAP409.1
    • AAP410.1
    • AAT509.1
    • AAT540.1
    • AAT571.1
    • AAT572.1
    • AAT577.1
    • AAT579.1
    • AAT582.1
    • AAT626.1
    • AAT634.1
    • AAT652.1
    • AAT657.1
    • AAT660.1
    • AAT722.1
Amount recalled
3,119 devices

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new St. Jude Medical, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 16, 2020 · Data as of Sep 19, 6:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.