Reported Mar 22, 2017 · Terminated

C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller; Cryosurgical Unit, Cryogenic Surgical…

C2 Therapeutics, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: C2 Therapeutics, Inc. · 303 Convention Way Ste 1 · Redwood City, CA · 94063-1415

Is this the product you have?

  • C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller; Cryosurgical Unit, Cryogenic Surgical Device The affected product is the Controller Cap component only, which is provided to the customer already assembled onto the Controller
  • Model numberFG-1012
  • Product UsageThe C2 CryoBalloon Ablation System is intended for use as a cryosurgical tool in the field of general surgery, specifically for endoscopic applications, to include ablation of Barrett s Esophagus with dysplasia. It is a cryosurgical system with a nitrous oxide cooled balloon that is compatible with a commercially available endoscope with a minimum working channel inner diameter (ID) of 3.7 mm and length of 100 cm. The C2 CryoBalloon System is a system comprised of a Catheter (sterile), Controller (non-sterile), and Cartridge (non-sterile). The Device is used to ablate unwanted tissue by application of extreme cold. The balloon at the distal end of the Catheter comes in contact with tissue and is inflated with nitrous oxide. Tissue is visualized through the inflated balloon, and the treatment site is selected by adjusting the endoscope and Controller position. The nitrous oxide spray cools the balloon to ablate the unwanted tissue, and the nitrous oxide exhausts through the Controller
Lot codes and dates
  • All lots distributed between June 23, 2016 and December 20, 2016: UPDATE - expanded to include product distributed from February 1 2016 through February 8, 2017. All numbers below have been updated
  • Lot numbers

    89 of 89 codes

    • Expiry dates 01122016-02 12-Jul-16
    • 06242016-01 1-Jan-2017
    • 11282016-03 2-Jun-2017
    • 01042016-03 14-Jul-16
    • 06292016-02 6-Jan-2017
    • 09202016-01 21-Mar-2017
    • 07062016-01 8-Jan-2017
    • 09222016-01 23-Mar-2017
    • 01252016-02 02-Aug-16
    • 07082016-02 13-Jan 2017
    • 09232016-01 28-Mar-2017
    • 01282016-01 01-Aug-16
    • 07082016-03 14-Jan-2017
    • 09232016-02 27-Mar-2017
    • 01292016-01 02-Aug-16
    • 07152016-01 21-Jan-2017
    • 09292016-01 4-Apr-2017
    • 02022016-03 09-Aug-16
    • 07152016-02 20-Jan-2017
    • 09302016-03 4-Apr-2017
    • 02082016-01 09-Aug-16
    • 07212016-01 25-Jan-2017
    • 10052016-02 19-Apr-2017
    • 02092016-02 11-Aug-16
    • 07252016-01 28-Jan-2017
    • 10142016-01 18-Apr-2017
    • 02112016-02 17-Aug-16
    • 07262016-01 9-Feb-2017
    • 10192016-01 24-Apr-2017
    • 02172016-02 25-Aug-16
    • 07282016-02 2-Feb-2017
    • 10212016-01 25-Apr-2017
    • 02222016-01 26-Aug-16
    • 08022016-01 17-Feb-2017
    • 10242016-01 26-Apr-2017
    • 03012016-01 04-Sep-16
    • 08032016-02 5-Feb-2017
    • 10262016-02 1-May-2017
    • 03072016-01 10-Sep-16
    • 08112016-01 16-Feb-2017
    • 10282016-02 8-May-2017
    • 03102016-02 15-Sep-16
    • 08232016-01 26-Feb-2017
    • 11022016-01 9-May-2017
    • 03152016-03 21-Sep-16
    • 08262016-01 2-Mar-2017
    • 11042016-01 10-May-2017
    • 03282016-02 29-Sep-16
    • 09022016-01 8-Mar-2017
    • 11092016-01 15-May-2017
    • 03292016-01 31-Sep-16
    • 09092016-01 14-Mar-2017
    • 11142016-02 16-May-2017
    • 09122016-02
    • 15-Mar-2017
    • 11152016-02 18-May-2017
    • 04012016-01 06-Oct-16
    • 09192016-01 19-Mar-2017
    • 11162016-01 21-May-2017
    • 09192016-02 21-Mar-2017
Amount recalled
755 controller caps

Where it was sold

  • Nationwide

Why it was recalled

The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is tightened onto the controller. That could compromise the integrity and result in damage to the Controller Cap.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 13, 2017 · Data as of Sep 19, 5:31 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.