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

Recall Z-2485-2025 — Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect Decompression System 10MM, VF Implant 101-9810 00884662000536 Superion Indirect Decompression System 12MM, VF Implant 101-9812 00884662000543 Superion Indirect Decompress

U.S. FDA — Device Enforcement · United States · 2025-06-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2485-2025
Date of alert
2025-06-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Boston Scientific Neuromodulation Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00884662000529
Reported risk: As a result of a comprehensive product performance review it was determine that the device and instruments are not consistently meeting expected performance levels. Issues include breakage of the instruments and implant/device.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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