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FDA (Device enforcement)Recalled 2024-07-09class ii

Medtronic Perfusion Systems: Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312

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).

Details from the source

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. Quantity: 290 units Lot/code info: GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065

UPC codes

20613994879329

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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