DLP Coronary Ostial Cannulae (Medtronic) – Sterile Packing Issue (2024)
Unsealed sterile packaging may potentially compromise the sterility of medical devices.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Brand
Medtronic Perfusion Systems
Lot Codes / Batch Numbers
GTIN 00613994576019, Lot Numbers: 2023070529, GTIN 20613994576013, Lot Numbers: 2023070529
Products Sold
GTIN 00613994576019, Lot Numbers: 2023070529; GTIN 20613994576013, Lot Numbers: 2023070529
Medtronic Perfusion Systems is recalling Medtronic DLP Coronary Ostial Cannulae, Model Number 30050 due to Potential for unsealed sterile packing.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for unsealed sterile packing.
Recommended Action
Per FDA guidance
Medtronic issued an Urgent Medical Device Recall notice to its consignees on 03/19/2024 via letter (UPS). The notice explained the issue, potential risk, and requested the consignee identify and return the product. Consignee was directed to forward the notice to all affected parties. For questions, the consignee was directed to contact their Medtronic field representative.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026