Medical device recalls Moderate risk

Elekta, Inc. recalls MOSAIQ Oncology Information System

Recall date
June 17, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2052-2016
FDA classification
Class II
Brand / firm
Elekta, Inc.
Sold / distributed
US Distribution including Puerto Rico and to the states of : AK, AZ, CA, FL, GA, IL, IN, LA, MD, MI, MO, NJ, NY, OH, OR, PA, TN, TX, UT, VA, WA, and to the countries of : Canada, Denmark, Finland, Germany, Israel, Japan, Netherlands, Norway, Sweden, United Kingdom

Why it was recalled

It is possible that that the selected Plan-of-the Day could be accidently changed by scrolling the mouse wheel up and down and inadvertently selecting another plan.

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

What was recalled

MOSAIQ Oncology Information System

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