FDA Device recall Z-2472-2012
Marathon Flow Directed Micro Catheter, Model #105-5055
- FDA Device
- Class II
- terminated
- Published 2012-10-03
On 2012-10-03 the FDA classified a Class II recall of Marathon Flow Directed Micro Catheter, Model #105-5055 by Micro Therapeutics, citing the recall was initiated because ev3 Neurovascular has identified one lot of UltraFlow Flow Directed Micro Catheters and Marathon Flow Directed Micro Catheters may have been misla….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2472-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2011-09-23 |
| Published | 2012-10-03 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Micro Therapeutics |
| Distribution | US |
Product
Marathon Flow Directed Micro Catheter, Model #105-5055. Product Usage: The Marathon Flow Directed Micro Catheter is intended to access the peripheral and neuro vasculature for the controlled selective infusion of physician-specified therapeutic agents such as embolization materials and of diagnostic materials such as contrast media.
Reason
The recall was initiated because ev3 Neurovascular has identified one lot of UltraFlow Flow Directed Micro Catheters and Marathon Flow Directed Micro Catheters may have been mislabeled.
Identifiers
| code_info | Lot # 9374210 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2472-2012%22
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