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

Recall Z-2428-2021 — Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB

U.S. FDA — Device Enforcement · United States · 2021-07-21 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2428-2021
Date of alert
2021-07-21
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Cordis Corporation
Product category
device
Product type
Devices
Reported risk: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a manner that may allow entrapment of the catheter between endovascular devices and the vessel wall, which can lead to marker band movement or dislodgement.
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.