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FDA (Device enforcement)Recalled 2025-02-21class i

MEDLINE INDUSTRIES, LP - Northfield: Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF

Hazard

Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

Details from the source

Reason for recall: Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula. Distribution: US: CA, FL, MN, NY, OH, OR, PA, TX, WV Quantity: 320 units Lot/code info: HEART BASIN PACK-LF, UDI/DI 10195327563561 (ea) 40195327563562 (case), Lot Numbers 24BMB798, 24DMH381, 24EMF949, 24GMF161, 24IMB237.

UPC codes

10195327563561, 40195327563562

Source

Official record: FDA (Device enforcement)

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

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