Data Foundry

Medical device recalls 2017

PM 1250 and PM 2250 ZENEX — Class II medical device recall Z-0036-2018

Terminated recall by St Jude Medical Inc., reported 2017-10-25. New pacemaker firmware was developed to further mitigate the risk of unauthorized access to our pacemakers tha

Recall numberZ-0036-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSt Jude Medical Inc., Sylmar, CA, United States
Recall initiated2017-08-28
Classified2017-10-19
Reported by FDA2017-10-25
Terminated2020-07-08
Quantity4,828 units
Reason classessoftware
Serial numbers2811898, 2811899, 2811900, 2811901, 2811902, 2811903, 2811904, 2811905, 2811906, 2811907, 2811908, 2811909, 2811910, 2811911, 2811912, 2811913, 2811914, 2811915, 2811916, 2811917, 2811918, 2811919, 2811920, 2811921, 2811922 and 475 more

Product

PM 1250 and PM 2250 ZENEX; PM1282 and PM2282 ZENEX MRI These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. These devices are used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders.

Reason for recall

New pacemaker firmware was developed to further mitigate the risk of unauthorized access to our pacemakers that utilize radio frequency (RF) communications.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0036-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.