FDA Device recall Z-0210-2024
Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork fo…
- FDA Device
- Class II
- ongoing
- Published 2023-11-08
On 2023-11-08 the FDA classified a Class II recall of Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork fo… by Maquet Cardiovascular, citing device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0210-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-19 |
| Published | 2023-11-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Maquet Cardiovascular |
| Distribution | AL, AR, CA, FL, GA, IN, KY, MI, NJ, OK, PA, TN, TX |
Product
Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).
Reason
Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.
Identifiers
| code_info | UDI-DI: 00607567700239, Lot: 3000313857. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0210-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.