Recall StatusTerminated
Date Initiated2021-11-22
Date Terminated2023-08-31
Product Quantity711 units
Reason for Recall
Under certain circumstances, the WIRION filter assembly may become difficult to withdraw. Under such circumstances, alternative means may be necessary for withdrawal and the device may be prone to tearing or separating which may result in a risk for embolization.
Firm Action
Consignees were issued an URGENT: Medical Device Recall letter dated 11/22/2021.
Consignees are asked to immediately remove from use and return affected devices to CSI. To do so:
1) Complete the attached Customer Acknowledgement Form.
a) Per lot, document the quantity of all devices that are to be returned.
b) Per lot, document the quantity of all devices that have been consumed.
2) Place the Acknowledgement Form with the device.
3) Return the device and Acknowledgement Form to CSI using the pre-paid label.
A CSI Sales representative can return the device and form. Please contact CSI Recall Coordinator to organize pick up and return of the product.
If all products specified in this recall notice have previously been consumed, used or are no longer available for return to CSI, please complete the Customer Acknowledgement Form per the above, and return the form to CSI in the provided envelope.
For further info, please contact:
Cardiovascular Systems, Inc.
Field Action Hotline
[email protected]
651-259-2800
Distribution Pattern
United States- AK, AL, AR, AZ, CA, DC, FL, GA, GU, HI, IA, IL, IN, KY, LA, MA, MI, MN, MO, MS, ND, NE, NH, NJ, NM, NV, NY, OH, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV
OUS - Netherlands
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.