Myelotec Video Guided Catheters — Class II medical device recall Z-2779-2017
Ongoing recall by Myelotec, Inc., reported 2017-08-09, distributed in CA, FL, KY, MN, NJ. Obstructed/blocked port from defective VGC Access Port Body component.
| Recall number | Z-2779-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Myelotec, Inc., Roswell, GA, United States |
| Recall initiated | 2017-03-02 |
| Classified | 2017-07-28 |
| Reported by FDA | 2017-08-09 |
| Distributed | CA, FL, KY, MN, NJ |
| Countries outside the US | BR, IR, KR, KW, MY, SG, TR, TW |
| Quantity | 2,980 units |
| Lot numbers | 4123/MY33613, 4250/MY06614, 4279/MY06614, 4305/MY10814, 4331/MY13914, 4331/MY25214 |
| Model numbers | 2010, 3.0 |
Product
Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels
Reason for recall
Obstructed/blocked port from defective VGC Access Port Body component.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2779-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.