Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
- Company
- Medtronic Perfusion Systems
- Recall Initiated
- July 9, 2024
- Posted
- September 12, 2024
- Recall Number
- Z-3128-2024
- Quantity
- 290 units
- Firm Location
- Brooklyn Park, MN
Reason for Recall
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).
Distribution
Worldwide distribution - US Nationwide and the countries of Cambodia, Greece, Ireland, Italy, Saudi Arabia, Switzerland, United Kingdom, Viet Nam.
Lot / Code Info
GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065
Root Cause
Under Investigation by firm
Action Taken
Medtronic issued an Urgent: Medical Device Recall notice to its consignees on 07/09/2024 via UPS. The notice explained the issue, potential risk, and requested return of the affected device. Those who further distributed the device were directed to share the notice with those to whom the affected product was distributed.