Reported Jul 4, 2018 · Terminated

Unify, Sterile EO, Model #/ Part #

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. · 15900 Valley View Ct · Sylmar, CA · 91342-3577

Is this the product you have?

Unify, Sterile EO, Model #/ Part #

6 of 6 products

Products covered by this recall
#Product as published
1CD3231-40/100029240, 100030104, 100041904
2CD3231-40Q/100029281, 100030124, 100041905
3CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009
4CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010
5CD3281-40Q/100056770
6CD3297-40/100056933
Lot codes and dates
  • Serial #:

    3,952 of 3,952 codes

    • 1015752
    • 730063
    • 739101
    • 737664
    • 1100971
    • 1220399
    • 1220292
    • 1220290
    • 1220402
    • 1220289
    • 1220397
    • 1220296
    • 790402
    • 1220298
    • 1220297
    • 1220302
    • 1220398
    • 1220300
    • 1220304
    • 1011008
    • 1045234
    • 727133
    • 727125
    • 1015722
    • 769238
    • 782698
    • 806935
    • 1203620
    • 824778
    • 1194681
    • 1194692
    • 1142920
    • 1142348
    • 1142916
    • 761491
    • 763173
    • 768968
    • 746500
    • 773404
    • 790396
    • 807191
    • 805967
    • 761487
    • 769242
    • 749537
    • 761680
    • 720899
    • 788660
    • 769286
    • 782672
    • 761268
    • 784460
    • 825005
    • 717555
    • 736459
    • 810157
    • 805939
    • 815815
    • 824979
    • 790367
Amount recalled
40738

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

  • Nationwide

Why it was recalled

The firm is releasing new firmware for high voltage implantable cardiac devices (ICD) and cardiac resynchronization therapy defibrillators (CRT-D) intended to strengthen security by providing an additional layer of protection against unauthorized device access. For older generation devices not capable of accepting the firmware, the firm is advising customers of the option to permanently disable the RF communication capability in these devices.

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 Mar 8, 2024 · Data as of Sep 19, 5:29 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.