Recall StatusTerminated
Date Initiated2015-12-31
Date Terminated2016-08-25
Product Quantity1,985 units
Reason for Recall
Incorrect cannula of the sheath introducer (smaller than intended).
Firm Action
The firm, Cordis, sent an 'Urgent MEDICAL DEVICE CORRECTION (Field Safety Notice) dated 12/31/2015 to its customers. The notice described the product, problem and actions to be taken. The customers were instructed to do the following:
1) Read the Description of the problem section carefully to fully understand the
issue involved.
2) Check your inventory to determine if you have any remaining affected product
in your possession. Check all storage and usage locations. The purpose is to
identify the product, not to remove the product.
3) Keep a copy of this notice with any affected product.
4) Review, complete, sign and return the enclosed Acknowledgement Form
directly to Cordis by fax to (908) 429-8287 Alternate fax (904) 928-5077. number or scan and email to
[email protected].
5) Share this letter with anyone who needs to be informed in your facility and in any facility where potentially affected devices may have been transferred.
6) Maintain awareness of this notice until all affected product has been
consumed. If vessel dilator to sheath incompatibility is experienced, you can
report the incident through the standard complaint process (1-800-327-7714
Option 3).
For any health care professional with medical concerns, please contact
Cordis to speak to a clinician at 1-800-327-7714 Option 3, Monday
through Friday from 9:00 AM to 5:00 PM EST.
For questions related to the Correction that are not adequately addressed
in this letter, please contact the Cordis Field Action Coordinator at (786) 313-2365.
For questions related to the Acknowledgement Form and its return, please
contact Cordis QA at (786) 313-8730."
Root Cause
Mixed-up of materials/components
Distribution Pattern
US Nationwide Distribution including states of:AL, AZ, CA, CO, CT, FL, GA, IN, KY, LA, MA, MD, MI, MN, MO, MT, NC, NH, NJ,NY, OH, OR, PA, RI, TN, TX, VA, WA, WV, and Hawaii.
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.