Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Reason for recall: Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000. Distribution: US Nationwide distribution. Quantity: 22 kits Lot/code info: UDI/DI 40195327185078 (case), 10195327185077 (each), Lot Numbers: 24BMF235
40195327185078, 10195327185077
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.