FDA Medical Device Recalls (openFDA)
Medtronic Perfusion Systems: Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
- Recall number
- Z-0986-2025
- Recalling firm
- Medtronic Perfusion Systems
- Product
- Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
- Status
- Open, Classified
- Initiated
- 2024-12-12
- Posted
- 2025-01-17
- Terminated
- not on file
- Reason
- Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
- Root cause
- Packaging
- Action
- An URGENT: MEDICAL DEVICE RECALL notification letter dated 12/12/24 was sent to customers. Patient Recommendations: Patients previously supported with an impacted device face no additional risk from the issue described in this communication and should continue to be monitored per your practice s normal follow-up procedures. Customer Actions: Medtronic requests that you take the following actions: " Review your inventory for listed product. " Immediately identify and quarantine all unused, listed product in your inventory. " Return unused, listed product in your inventory to Medtronic by contacting Customer Service at 1-800-854-3570, Option 1 then Option 4, and referencing this communication to initiate a return and credit of unused product. Your Medtronic sales representative can assist you in the return of affected product as necessary. " Complete the enclosed Customer Confirmation Form and email to RS.CFQFCA@medtronic.com. This form must be returned even if you do not have any affected product in your possession. " Please share this notification with others in your organization as appropriate. If product listed above has been forwarded to another facility, please notify the facility of this . " Please maintain a copy of this communication in your records. If you have any questions regarding this communication, please contact your Medtronic Field Representative.
- Quantity
- 440 units
- Distribution
- Worldwide - US Nationwide distribution.
- Lot, serial or model codes
- Model 72422 UDI-DI: 20643169485970, Lot Numbers: 2023071075, 202309C075
- 510(k) numbers
- ["K840002"]
- PMA numbers
- not on file
- Product code
- DWF
- Firm FEI
- 1000116158
- Firm city
- Brooklyn Park
- 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