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FDA Medical Device Recalls (openFDA)

Maquet Cardiovascular, LLC: Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.

Recall number
Z-0724-2024
Recalling firm
Maquet Cardiovascular, LLC
Product
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.
Status
Open, Classified
Initiated
2023-12-01
Posted
2024-01-12
Terminated
not on file
Reason
Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may result in polyimide particulate matter being introduced into the arterial conduit for patients undergoing a coronary artery bypass graft (CABG) or peripheral bypass graft surgery.
Root cause
Component design/selection
Action
An Urgent Medical Device Correction notice dated December 1, 2023 was sent via FedEx 2-Day delivery. Please examine your inventory immediately to determine if you have any of the product codes and lot numbers listed in the notice and remove these from use. Return any unused/unexpired affected product to Maquet/Getinge. Please forward this information to all current and potential VasoView HemoPro EVH System users within your hospital / facility. If you are a distributor who has shipped any affected products to customers, please forward this document to their attention for appropriate action. If you have any questions, please contact your Maquet/Getinge representative or call the Maquet/Getinge Customer Support at 888-880-2874, Monday through Friday, between the hours of 6 AM to 5 PM (Pacific Standard Time). Whether or not your facility has affected product listed in the notice, please complete and sign the MEDICAL DEVICE REMOVAL - RESPONSE FORM to acknowledge that you have received the notification. Return the completed form to Maquet/Getinge by e-mailing a scanned copy to VVHemoProParticulate2023.act@getinge.com or by faxing the form to 1-800-878-9105.
Quantity
38,094 units (US)
Distribution
US: OUS: China, Brazil, Hong Kong.
Lot, serial or model codes
UDI-DI: 00607567701250, Lots: 3000279266, 3000280189, 3000281082, 3000281083, 3000281381, 3000282927, 3000283156, 3000281741, 3000286706, 3000287254, 3000288363, 3000288576, 3000289020, 3000289548, 3000289927, 3000290482, 3000291429, 3000291157, 3000291645, 3000292098, 3000293522, 3000293788, 3000293823, 3000295050, 3000294365, 3000295346, 3000296172, 3000296021, 3000296498, 3000297028, 3000300016, 3000299854, 3000300155, 3000300260, 3000301042, 3000301666, 3000302760, 3000303282, 3000303854, 3000304912, 3000304645, 3000306277, 3000306437, 3000307090, 3000307871, 3000308725, 3000310691, 3000311127, 3000311525, 3000311892, 3000312494, 3000312722, 3000314373, 3000314821, 3000316023, 3000316027, 3000316024, 3000317576, 3000317501, 3000317575, 3000318901, 3000318302, 3000320140, 3000320141, 3000320773, 3000320773, 3000321483, 3000321723, 3000323214, 3000324409, 3000324397, 3000325013, 3000325249, 3000325689, 3000325776, 3000328206, 3000328561, 3000329723, 3000328562, 3000330445, 3000331131, 3000331388, 3000332428, 3000332510, 3000332993, 3000333524, 3000333829, 3000334315, 3000335670, 3000336708, 3000337272, 3000339701, 3000340534, 3000341675, 3000341133, 3000342250, 3000342251, 3000343266, 3000343264, 3000344887, & 3000351187.
510(k) numbers
["K153194"]
PMA numbers
not on file
Product code
GEI
Firm FEI
2242352
Firm city
Wayne
Firm state
NJ
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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