Recall of Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000) with Lot 3000547797 due to potential exposure to improper sterilization during gamma processing.
Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run ID 1183-28782A) performed by STERIS at its Whippany, NJ facility between March 31 and April 1 of 2026.
Maquet is recalling the Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000) with Lot 3000547797 because it may have been exposed to an incorrect sterilization dose during gamma processing. This could affect the device's safety and sterility.
The device may have been exposed to an out-of-specification sterilization dose during a gamma sterilization run at STERIS in Whippany, NJ. This could compromise the device's sterility and safety.
Medical professionals using the Vasoview Hemopro 2 system for vessel harvesting procedures are most at risk if they have the specific lot number 3000547797.
Check for the lot number 3000547797 on the Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000) with UDI 00607567700406.
Look for the lot number 3000547797 on the Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000).
The Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run at STERIS in Whippany, NJ.
The recall record does not specify a remedy, so contact Maquet Cardiovascular directly for guidance.
The recall indicates potential issues with sterilization, but the record does not confirm if the device is unsafe for use.
We’ve drafted a message you can send Maquet Cardiovascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2741-2026 — Maquet Cardiovascular Maquet Cardiovascular Hello, I own a Maquet Cardiovascular that is covered by recall Z-2741-2026 from Maquet Cardiovascular. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
