Medtronic recalls 2090 Programmers with serial number prefixes PKK0 and PKK1 that may move cursor autonomously when Finger Touchscreen is enabled in software version 3.2 or higher. Affected units include specific model variants and GTINs.
Medtronic CareLink 2090 programmers with serial number prefixes PKK0 and PKK1 have the potential for autonomous cursor motion when Finger Touchscreen capability is enabled by software version 3.2 or higher.
Medtronic is recalling 2090 Programmers with serial number prefixes PKK0 and PKK1. These devices may move the cursor automatically when Finger Touchscreen capability is enabled in software version 3.2 or higher, potentially causing unintended actions.
When Finger Touchscreen capability is enabled in software version 3.2 or higher, the device may move the cursor autonomously. This could lead to unintended actions on the device, such as changing settings or triggering functions without user input.
Users of Medtronic CareLink 2090 Programmers with serial number prefixes PKK0 and PKK1 are affected. Patients using these devices for medical monitoring are most at risk if they experience unintended cursor movements.
Check for serial number prefixes PKK0 or PKK1 on the device. Affected models include specific variants like 2090, 209031, 2090AA, and others listed in the recall. Also check the GTIN numbers provided in the recall notice.
Disable Finger Touchscreen capability in software version 3.2 or higher to prevent unintended cursor movement.
Affected models include 2090, 209031, 2090AA, 2090AA4, 2090AC, 2090AM, 2090CHEN, 2090CHFR, 2090CL, 2090EN, 2090FR, 2090LDEN, 2090NL, 2090W, 2090WCHDE, 2090WCHEN, 2090WCHFR, 2090WDE, 2090WFR, 2090WLD, and 2090WNL with serial number prefixes PKK0 and PKK1.
Check if your device has a serial number prefix of PKK0 or PKK1. Affected units also include specific GTIN numbers listed in the recall notice.
Disable Finger Touchscreen capability in software version 3.2 or higher to prevent unintended cursor movement. No additional action is required beyond this step.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-3152-2024 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-3152-2024 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.
