Reported Mar 22, 2017 · Terminated

VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage: The VASOVIEW HEMOPRO VH-3500 is designed…

Maquet Cardiovascular, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Maquet Cardiovascular, LLC · 45 Barbour Pond Dr · Wayne, NJ · 07470-2094

Is this the product you have?

  • VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC
  • VESSEL HARVESTING SYSTEM Product UsageThe VASOVIEW HEMOPRO VH-3500 is designed for use in conjunction with the 7-mm Endoscope and is intended for specific use with the VASOVIEW HEMOPRO Power Supply
Lot codes and dates
    • 25126012
    • 25126080
    • 25126250
    • 25126375
    • 25126542
    • 25126659
    • 25128301
    • 25128602
    • 25128820
    • 25128905
    • 25129016
    • 25129155
    • 25129199
    • 25129239
    • 25129286
    • 25129335
    • 25129416
    • 25129513
Amount recalled
4283 units

Where it was sold

  • Nationwide

Why it was recalled

Maquet has received several complaints involving the VASOVIEW HEMOPRO VH-3500 which involve the device exhibiting the failure mode of intermittent or no power.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 12, 2018 · Data as of Sep 19, 6:16 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.