Medtronic recalls specific dual chamber pacemaker models (RED01, REDR01, REVDD01) distributed 2017-2019 that may experience circuit errors affecting device function. Owners should contact Medtronic for details.
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 (RED01, REDR01, REVDD01) made between March 2017 and January 2019. These devices may have circuit errors that affect their function if programmed for dual chamber mode with atrial sensing.
These pacemakers may experience a circuit error when programmed for dual chamber mode with atrial sensing. This error can affect device functionality, but does not cause immediate harm to the user.
People with Medtronic dual chamber pacemakers (VDD) that were programmed for dual chamber mode with atrial sensing between March 2017 and January 2019. Those with the specific model numbers RED01, REDR01, or REVDD01 are most at risk.
Check if your device is a Medtronic dual chamber pacemaker (VDD) with model numbers RED01, REDR01, or REVDD01. The recall covers devices distributed between March 2017 and January 2019.
Reach out to Medtronic for specific guidance on your device model and whether a fix is needed.
The recall does not require stopping use; it involves checking for circuit errors that may need correction.
Models RED01, REDR01, and REVDD01 distributed between March 2017 and January 2019.
Check your device model number against RED01, REDR01, or REVDD01 and verify the distribution date was 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-0808-2019 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0808-2019 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.
