Medical device recalls Moderate risk

Wilson-Cook Medical Inc. recalls Hemospray Endoscopic Hemostat

Recall date
July 24, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2541-2019
FDA classification
Class II
Brand / firm
Wilson-Cook Medical Inc.
Sold / distributed
Nationwide distribution to CA, CO, CT, FL, IL, IN, KY, LA, MN, MO, NC, NJ, NY, OH, PA, RI, SD, TX, VA, WA. International distribution to Canada, Austria, Belgium, Cyprus, Denmark, France, Germany, Greece, Italy, Portugal, Spain, and United Kingdom.

Why it was recalled

Potential for Hemospray device to be unable to spray powder due to misassembly of devices.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Hemospray Endoscopic Hemostat

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