Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-3152-2024 — 2090 Programmers with serial number prefixes PKK0 and PKK1: a) 2090, Product Description: PRGM 2090 PROGRAMMER-PORTABLE CRM; b) 209031, Product Description: PROGRAMMER 209031 PORTABLE CRM; c) 2090AA, Product Description: PROGRAMMER 2090AA PORTABLE CRM; d) 2090AA4, Product Description:

U.S. FDA — Device Enforcement · United States · 2024-07-11 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-3152-2024
Date of alert: 2024-07-11
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medtronic Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00613994136480

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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