Medtronic DLP Single Stage Venous Cannulae with right recall
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Why was Medtronic DLP Single Stage Venous Cannulae with right recalled?
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
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 20613994879329, Lot Numbers: 2023090954, 202312C065
- Product
- Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
- Recalling firm
- Medtronic Perfusion Systems
- Quantity
- 290 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Cambodia, Greece, Ireland, Italy, Saudi Arabia, Switzerland, United Kingdom, Viet Nam.
- Recall date
- September 18, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)