Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Reported: May 22, 2024 Initiated: March 19, 2024 #Z-1795-2024
Product Description
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Reason for Recall
Potential for unsealed sterile packing.
Details
- Recalling Firm
- Medtronic Perfusion Systems
- Units Affected
- 250 units
- Distribution
- Worldwide distribution.
- Location
- Brooklyn Park, MN
Frequently Asked Questions
What product was recalled? ▼
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050. Recalled by Medtronic Perfusion Systems. Units affected: 250 units.
Why was this product recalled? ▼
Potential for unsealed sterile packing.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 22, 2024. Severity: Moderate. Recall number: Z-1795-2024.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11