Medtronic DLP Coronary Ostial Cannulae recall
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Why was Medtronic DLP Coronary Ostial Cannulae recalled?
Potential for unsealed sterile packing.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GTIN 00613994576019, Lot Numbers: 2023070529; GTIN 20613994576013, Lot Numbers: 2023070529
- Product
- Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
- Recalling firm
- Medtronic Perfusion Systems
- Quantity
- 250 units
- Distribution
- Worldwide distribution.
- Recall date
- May 22, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)