FDAApril 16, 2018device

Current, Sterile EO, Model #/ Part #: 1207-30/50020236-001, 60010739-207, 60010739-407; 1207-36/50020237-001, 60010742-207, 60010742-307, 60010742-407, 60010742-707; 2207-30/ 50020238-001, 60010738-207; 2207-36/ 50020239-001, 60010741-207, 60010741-307, 60010741-407, 60010741-707; CD1211-36/10000...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

st jude medical

UPCs

500202360016001073920760010739407500202370016001074220760010742307600107424076001074270750020238001600107382075002023900160010741207

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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