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

Magellan Robotic Catheter Accessory Kits, Model number MACC 50 and MACC80. Cardiology: The Hansen Medical Magellan System is a robotic control system that enables positioning and visualization of a Magellan Catheter and an off-the-shelf guide wire while allowing a physician to remain seated and — recall Z-1564-2016

U.S. FDA — Device Enforcement · United States · 2016-03-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1564-2016
Date of alert
2016-03-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Hansen Medical Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20151117
Reported risk: Firm's quarterly dose audit testing showed that one batch was radiated below the augmented dose and therefore did not meet the augmented dose of 28.4 kGy.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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.