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

Recall Z-1072-2025 — SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve Stimulation (VNS).

U.S. FDA — Device Enforcement · United States · 2024-12-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1072-2025
Date of alert
2024-12-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
LivaNova USA, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
05425025750405
Reported risk: Vagus nerve stimulator generators may stop delivering stimulation due to an internal, mechanically activated component that may become stuck in a closed position, which may result in patients returning to baseline seizure frequency or depressive symptoms and in the longer term, patients may be required to undergo generator replacement surgery to replace their device.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.