Maquet recalls VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System (Model C-VH-350: Lot 3000280189, 3000276183) due to unsterilized batches. Affected users should contact Maquet for details.
Some batches of product were not sterilized to their minimum sterilization specification.
Maquet is recalling some batches of the VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System because they weren't properly sterilized. This could lead to infections or other health risks if used without proper sterilization.
The device was not sterilized to the minimum required standard in some batches. This means the device could be contaminated with harmful bacteria, increasing the risk of infections or other health issues during medical procedures.
Users of the VASOVIEW HEMOPRO system who purchased the specific lot numbers (3000280189, 3000276183) are affected. Surgeons and medical professionals using this device are at highest risk.
Check the lot numbers on your VASOVIEW HEMOPRO system: 3000280189 or 3000276183. The product is sold under the brand Maquet Cardiovascular.
Identify if your VASOVIEW HEMOPRO system has lot numbers 3000280189 or 3000276183.
The recall states that some batches were not sterilized to the minimum specification, so affected units may pose a risk of infection. The official notice does not specify if the device is safe to use without action.
The recall record does not specify a remedy, so users should contact Maquet Cardiovascular directly for instructions.
Check the lot numbers on your VASOVIEW HEMOPRO system: 3000280189 or 3000276183.
We’ve drafted a message you can send Maquet Cardiovascular to request your refund or repair — edit it as you like.
Subject: Recall Z-1335-2023 — Maquet Cardiovascular Maquet Cardiovascular Hello, I own a Maquet Cardiovascular that is covered by recall Z-1335-2023 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.
