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U.S. Department of Health and Human Services

Class 2 Device Recall Vasoview Hemopro

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 Class 2 Device Recall Vasoview Hemoprosee related information
Date Initiated by FirmDecember 01, 2023
Date PostedJanuary 12, 2024
Recall Status1 Open3, Classified
Recall NumberZ-0724-2024
Recall Event ID 93615
510(K)NumberK153194 
Product Classification Electrosurgical, cutting & coagulation & accessories - Product Code GEI
ProductVasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.
Code Information 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.
FEI Number 2242352
Recalling Firm/
Manufacturer		 Maquet Cardiovascular, LLC
45 Barbour Pond Dr
Wayne NJ 07470-2094
For Additional Information ContactKenisha Williams
973-709-7860
Manufacturer Reason
for Recall		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.
FDA Determined
Cause 2		Component design/selection
ActionAn 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 in Commerce38,094 units (US)
DistributionUS: OUS: China, Brazil, Hong Kong.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database510(K)s with Product Code = GEI
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