Medical device recalls Moderate risk

CooperSurgical, Inc. recalls Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151

Recall date
March 12, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1879-2018
FDA classification
Class II
Brand / firm
CooperSurgical, Inc.
Sold / distributed
CA, SC, WI, MI, NH, MD, OH, NJ, Australia, France, Spain

Why it was recalled

Products have been packaged with an incorrect product size.

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

What was recalled

Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151

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