Medtronic Perfusion Systems Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312 Recall
Hazard assessment based on recall description.
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 Single Stage Venous Cannulae with right angle metal tip, REF 67312
Brand
Medtronic Perfusion Systems
Lot Codes / Batch Numbers
GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065
Products Sold
GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065
Medtronic Perfusion Systems is recalling Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312 due to During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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).
Recommended Action
Per FDA guidance
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.
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