Medtronic recalls specific dual chamber pacemakers (ATDR01, ATDRL1, ATDRS1) distributed 2017-2019 that may experience circuit errors if programmed for dual chamber mode with atrial-sensing.
A subset of Medtronic dual chamber pacemakers distributed worldwide between 10 March 2017 and 7 January 2019 under the brand names Adapta, Versa, and Sensia when programmed to a dual chamber mode with atrial-sensing, may experience a circuit error that affects device functionality
Medtronic is recalling certain dual chamber pacemakers that may have a circuit error when programmed for dual chamber mode with atrial-sensing. This could affect device functionality and potentially cause health issues if not addressed.
The circuit error may cause the pacemaker to malfunction when programmed for dual chamber mode with atrial-sensing. This could lead to improper heart rhythm management and potential health complications if the device does not function correctly.
Patients with Medtronic dual chamber pacemakers (models ATDR01, ATDRL1, ATDRS1) distributed between March 2017 and January 2019 are affected. Those with devices programmed for dual chamber mode with atrial-sensing are at higher risk.
Check if your pacemaker model is ATDR01, ATDRL1, or ATDRS1. These devices were distributed worldwide between March 2017 and January 2019. All serial numbers are affected.
Identify your pacemaker model number (ATDR01, ATDRL1, or ATDRS1) and check if it was distributed between March 2017 and January 2019.
The official recall notice does not specify which pacemakers are unaffected.
The official recall notice does not provide specific action steps for affected devices.
Check if your model is ATDR01, ATDRL1, or ATDRS1 and if it was distributed between March 2017 and January 2019.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0807-2019 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0807-2019 from Medtronic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
