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

Recall Z-2226-2023 — A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..

U.S. FDA — Device Enforcement · United States · 2023-06-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2226-2023
Date of alert
2023-06-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Neuromodulation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
643169738058
Reported risk: When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not available for download.
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.

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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.