C2 CryoBalloon Focal Catheter, REF FG-1009. C2 CryoBalloon Ablation System is used as a cryosurgical tool in the field of general surgery, specifically for endoscopic applications.
FDA Recall Z-2256-2018 · Posted 2018-06-05
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Recalling FirmPENTAX of America Inc
Recall StatusTerminated
Product CodeGEH
Date Initiated2018-03-30
Date Terminated2021-04-28
Product Quantity57 units
Reason for Recall
The catheter alignment arrow printed onto the strain relief is not aligned with the detachment feature of the catheter connector, resulting in the potential for the catheter to be attached to the controller in the detach orientation. In this orientation, the catheter is not securely attached to the controller and may be partially (~1cm) ejected from controller.
Firm Action
On 3/30/2018, C2 Therapeutics issued URGENT FIELD CORRECTION notices to customers via certified mail, return receipt requested.
Customers are advised to take the following Action:
- Forward a copy of the notice and the enclosures to the department in which is referenced in the notice.
- Inspect stock and quarantine products identified within the notice.
- The end user of the affected products should complete and return the response form via email to [email protected]. The response form contains an RMA number to allow for the return of devices affected by this field action, and enclosed in the package is a Federal Express shipping label for the returned merchandise.
Customers with questions can call 650-318-5899, Monday through Friday 8:30 AM - 5 PM, PST.
Root Cause
Vendor change control
Distribution Pattern
Distribution US nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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