Drug recall

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

FDA recall event 75428 · Class II · C.R. Bard, Inc.

Key facts

Event ID 75428
Recall numbers Z-0585-2017
Recalling firm C.R. Bard, Inc.
Product type Devices
Products 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.
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Defect; The contact part could possibly separate from the electrode affecting to functionality of the device.
Initiation date Oct 12, 2016
Report date Nov 23, 2016
Termination date Oct 5, 2021
City Covington
State GA
Country United States
FEI number 1018233

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

Browse all FDA drug and product recalls