FDA Device recall Z-1795-2024
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
- FDA Device
- Class II
- ongoing
- Published 2024-05-22
On 2024-05-22 the FDA classified a Class II recall of Medtronic DLP Coronary Ostial Cannulae, Model Number 30050 by Medtronic Perfusion Systems, citing potential for unsealed sterile packing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1795-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-19 |
| Published | 2024-05-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medtronic Perfusion Systems |
| Distribution | n/a |
Product
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Reason
Potential for unsealed sterile packing.
Identifiers
| code_info | GTIN 00613994576019, Lot Numbers: 2023070529; GTIN 20613994576013, Lot Numbers: 2023070529 |
|---|
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-1795-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.