FDA Device recall Z-2779-2017
Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels
- FDA Device
- Class II
- ongoing
- Published 2017-08-09
On 2017-08-09 the FDA classified a Class II recall of Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels by Myelotec, citing obstructed/blocked port from defective VGC Access Port Body component.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2779-2017 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-03-02 |
| Published | 2017-08-09 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Myelotec |
| Distribution | CA, FL, KY, MN, NJ |
Product
Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels
Reason
Obstructed/blocked port from defective VGC Access Port Body component.
Identifiers
| code_info | Lot No. 4123/MY33613, 4250/MY06614, 4279/MY06614, 4305/MY10814, 4331/MY13914, and 4331/MY25214 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2779-2017%22
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