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

Recall Z-3233-2017 — Platinium CRT-D 1741, Model Number TDF037U, UDI/GTIN 08031527015484, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients who are at high risk of

U.S. FDA — Device Enforcement · Italy · 2017-07-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3233-2017
Date of alert
2017-07-24
Country / jurisdiction
Italy
Risk level
Class II
Risk type
recall
Brand
Sorin Group Italia SRL - CRF
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08031527015484
Reported risk: There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) following an ElectroStatic Discharge (ESD) during the implant surgery or a Magnetic Resonance Imaging (MRI) scan, and what actions to take.
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.