Maquet recalls VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System (model C-VH-4000) due to unsterilized batches. Affected units have specific lot numbers. Consumers 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 2 Endoscopic Vessel Harvesting System because they weren't properly sterilized. This could lead to infections if used in medical procedures. The affected units have specific lot numbers listed in the recall.
The device was not sterilized to the required standard in some batches. This means the product could contain harmful bacteria or other contaminants that could cause infections during medical procedures.
Healthcare professionals using the VASOVIEW HEMOPRO 2 system for vascular surgery are most at risk. Patients undergoing procedures with this device may also be affected if the unsterilized batch is used.
Check the lot numbers on the device: 3000278401, 3000271148, 3000268643, 3000263026, 3000274504, 3000263925. The product is labeled as VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System with model number C-VH-4000.
Reach out to Maquet Cardiovascular for specific instructions on how to handle the affected units.
Some batches of the VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System were not sterilized to the minimum required specification.
Lot numbers 3000278401, 3000271148, 3000268643, 3000263026, 3000274504, and 3000263925.
Check the lot number on your device; if it matches the listed numbers (3000278401, 3000271148, 3000268643, 3000263026, 3000274504, 3000263925), it is affected.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1336-2023 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1336-2023 from Maquet. 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.
