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

Recall Z-2541-2020 — TactiCath Quartz Contact Force Ablation Catheter, Model Numbers: PN-004 065 (GTIN 07640157990033) and PN-004 075 (GTIN 07640157990040) - Product Usage: is a multi-electrode irrigated catheter with a deflectable tip designed to allow electrophysiological mapping of the heart and, when connected to a

U.S. FDA — Device Enforcement · United States · 2020-05-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2541-2020
Date of alert: 2020-05-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Abbott
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 07640157990033

Reported risk: High rate of reported complaints for the loss of contact force information while using the TactiCath Quartz Contact Force Ablation Catheter

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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