FDAFDA · Food and drugs·Recall number Z-1795-2024
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Published May 22, 2024 · Recall initiated: March 19, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Potential for unsealed sterile packing.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medtronic Perfusion Systems
- Distributor
- Worldwide distribution.
- Lot
- GTIN 00613994576019, Lot Numbers: 2023070529; GTIN 20613994576013, Lot Numbers: 2023070529
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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