Maquet Cardiovascular recalls

Recall found. Maquet Cardiovascular is named in FDA Class II recall Z-2741-2026 covering The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000. Hazard: 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. Identifying details: UDI 00607567700406, Serial/Lot Number 3000547797. Status: Ongoing.

Models with recalls

The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000 (1)

All Maquet Cardiovascular recalls

FDA Class II · Medical device · July 22, 2026

The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000 recall — Maquet Cardiovascular, LLC

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 1183-2878…

Official ID Z-2741-2026 · Official record ↗

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CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.