FDA Device recall Z-0986-2025
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
- FDA Device
- Class II
- ongoing
- Published 2025-01-29
On 2025-01-29 the FDA classified a Class II recall of Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr) by Medtronic Perfusion Systems, citing incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0986-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-12-12 |
| Published | 2025-01-29 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medtronic Perfusion Systems |
| Distribution | US |
Product
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Reason
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Identifiers
| code_info | Model 72422 UDI-DI: 20643169485970, Lot Numbers: 2023071075, 202309C075 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0986-2025%22
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