Medtronic 2090 Programmers with PKK0/PKK1 Serials May Cause Unintended Cursor Movement
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.
Use caution until it’s fixed
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.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/54670-medtronic-2090-programmers-with-pkk0-pkk1-serials-may-cause-unintended.
Source Summary by GovInfoNow · govinfonow.com/recall/54670-medtronic-2090-programmers-with-pkk0-pkk1-serials-may-cause-unintended · Updated August 19, 2026 · FDA enforcement record: FDA #Z-3152-2024
Cite this page
“Medtronic 2090 Programmers with PKK0/PKK1 Serials May Cause Unintended Cursor Movement.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54670-medtronic-2090-programmers-with-pkk0-pkk1-serials-may-cause-unintended. Based on FDA recall #Z-3152-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3152-2024%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Medtronic- Product
Medtronic Inc. recalls 2090 Programmers with serial number prefixes PKK0 and PKK1: a) 2090, Product Description: PRGM 2090 PROGRAMMER-PORTABLE- Category
Medical device
What to do — step by step
Check Device Settings
Disable Finger Touchscreen capability in software version 3.2 or higher to prevent unintended cursor movement.
How this recall unfolded
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
What models are affected by this recall?
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.
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Where this comes from
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.
- Official source: FDA Recall #Z-3152-2024 (July 11, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3152-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.