FDA Medical Device Recalls (openFDA)
Cardiovascular Systems Inc: WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6
- Recall number
- Z-0394-2022
- Recalling firm
- Cardiovascular Systems Inc
- Product
- WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6
- Status
- Terminated
- Initiated
- 2021-11-22
- Posted
- 2021-12-21
- Terminated
- 2023-08-31
- Reason
- 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.
- Root cause
- Device Design
- 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 csifieldactionhotline@csi360.com 651-259-2800
- Quantity
- 711 units
- Distribution
- 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
- Lot, serial or model codes
- Lot Numbers: Lot 67876, UDI 011085000049188217221221100000067876 Lot 70309, UDI 011085000049188217230110100000070309 Lot 68706, UDI 011085000049188217221227100000068706 Lot 69543, UDI 011085000049188217230103100000069543 Lot 75758, UDI 011085000049188217230203100000075758 Lot 77278, UDI 011085000049188217230210100000077278 Lot 79994, UDI 011085000049188217230223100000079994 Lot 81252, UDI 011085000049188217230301100000081252 Lot 81986, UDI 011085000049188217230307100000081986 Lot 83080, UDI 011085000049188217230313100000083080 Lot 81998, UDI 011085000049188217230320100000081998 Lot 84796, UDI 011085000049188217230327100000084796 Lot 87909, UDI 011085000049188217230411100000087909 Lot 89035, UDI 011085000049188217230418100000089035 Lot 86622, UDI 011085000049188217230404100000086622 Lot 90096, UDI 011085000049188217230424100000090096 Lot 93949, UDI 011085000049188217230515100000093949 Lot 91603, UDI 011085000049188217230501100000091603 Lot 94895, UDI 011085000049188217230521100000094895 Lot 91939, UDI 011085000049188217230507100000091939 Lot 101930, UDI 011085000049188217230717100000101930
- 510(k) numbers
- ["K210282"]
- PMA numbers
- not on file
- Product code
- NTE
- Firm FEI
- 3004742232
- Firm city
- Saint Paul
- Firm state
- MN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28