Maquet Cardiovascular, LLC 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). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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).
Brand
Maquet Cardiovascular, LLC
Lot Codes / Batch Numbers
UDI-DI: 00607567700239, Lot: 3000313857.
Products Sold
UDI-DI: 00607567700239, Lot: 3000313857.
Maquet Cardiovascular, LLC is recalling Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, in due to Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.
Recommended Action
Per FDA guidance
An Urgent Medical Device Removal notice was sent October 06, 2023 advising customers examine inventory, stop using, and remove any affected product from areas of use and return it to Getinge through Customer Service (888) 880-2874 between 6:00AM - 5:00PM PST. The notification should be forwarded to any system users and to any customers to which product was further distributed to. Complete and return the acknowledgement form to VV6proPkg2023.act@getinge.com or fax to (866) 326-9165.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AR, CA, FL, GA, IN, KY, MI, NJ, OK, PA, TN, TX
Page updated: Jan 10, 2026