FDAFDA · Food and drugs·Recall number Z-3128-2024
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Published September 18, 2024 · Recall initiated: July 9, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medtronic Perfusion Systems
- Distributor
- Worldwide distribution - US Nationwide and the countries of Cambodia, Greece, Ireland, Italy, Saudi Arabia, Switzerland, United Kingdom, Viet Nam.
- Lot
- GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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