Reported Jul 19, 2017 · Terminated

Infinity 7, Implantable Pulse Generator, REF 6662, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic…

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 7, Implantable Pulse Generator, REF 6662, Rx only
  • STERILE EO Product UsageThe Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic circuitry to generate constant-current electrical stimulation. The IPG is conductive on all sides, which allows the IPG case (also called a can) to be used as an anode for monopolar stimulation. The IPG communicates wirelessly with system programmers and controllers, and IPGs are available in small and large sizes to accommodate different power needs
Lot codes and dates
  • 373 of 373 codes

    • AAP149.1
    • AAP193.1
    • AAU029.1
    • ABA964.1
    • ACK581.1
    • ACK583.1
    • ACK784.1
    • ACK837.1
    • ACP794.1
    • ACT563.1
    • ACT591.1
    • ACT632.1
    • ACT645.1
    • ACT654.1
    • ACT684.1
    • ACT737.1
    • ACT895.1
    • ACU006.1
    • ACU060.1
    • ACU081.1
    • ACU085.1
    • ACU091.1
    • ACU165.1
    • ACU216.1
    • ACU220.1
    • ACU247.1
    • ADD484.1
    • ADD593.1
    • ADD633.1
    • ADD635.1
    • ADD647.1
    • ADD654.1
    • ADD668.1
    • ADD673.1
    • ADD681.1
    • ADD739.1
    • ADD754.1
    • ADD785.1
    • ADD786.1
    • ADD792.1
    • ADD808.1
    • ADD897.1
    • ADD904.1
    • ADD905.1
    • ADD910.1
    • ADD915.1
    • ADD946.1
    • ADD947.1
    • ADD970.1
    • ADD985.1
    • ADD995.1
    • ADE002.1
    • ADE014.1
    • ADE027.1
    • ADE030.1
    • ADE032.1
    • ADE073.1
    • ADE100.1
    • ADE104.1
    • ADE105.1
Amount recalled
373 units

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

The firm discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.

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.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 24, 2022 · Data as of Sep 19, 4:47 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.