Medical device recalls Moderate risk

C.R. Bard, Inc. recalls C-Max" Cutting Loop Electrodes, Storz One-Stem, 24 Fr, .014in., .35 mm, Sterile, Rx only, Manufactured by: C.R. Bard, I…

Recall date
October 12, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0585-2017
FDA classification
Class II
Brand / firm
C.R. Bard, Inc.
Sold / distributed
FL, GA, LA, OH, VA and WA.

Why it was recalled

Defect; The contact part could possibly separate from the electrode affecting to functionality of the device.

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

What was recalled

C-Max" Cutting Loop Electrodes, Storz One-Stem, 24 Fr, .014in., .35 mm, Sterile, Rx only, Manufactured by: C.R. Bard, Inc., Covington, GA 30014.

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