Medline has identified the presence of particulate within the fluid path of the Manifolds.
Reason for recall: Medline has identified the presence of particulate within the fluid path of the Manifolds. Distribution: US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK. Quantity: 322460 kits Lot/code info: Medline Kit Number/SKU 60010195: UDI/DI each 10193489040234, UDI/DI case 40193489040235, Lot Number: 24CBF820; Medline Kit Number/SKU 60010195: UDI/DI each 10193489040234, UDI/DI case 40193489040235, Lot Number: 24DBR149; Medline Kit Number/SKU 60010195: UDI/DI each 10193489040234, UDI/DI case 40193489040235, Lot Number: 24HBO437; Medline Kit Number/SKU 60010195: UDI/DI each 10193489040234, UDI/DI case 40193489040235, Lot Number: 24IBJ827; Medline Kit Number/SKU 60010195: UDI/DI each 10193489040234, UDI/DI case 40193489040235, Lot Number: 25ABI082; Medline Kit Number/SKU 60033123: UDI/DI each 10193489042436, UDI/DI case 40193489042437, Lot Number: 25BBI613; Medline Kit Number/SKU 60033123: UDI/DI each 10193489042436, UDI/DI case 40193489042437, Lot Number: 25BBR862; Medline Kit Number/SKU 60033123: UDI/DI each 10193489042436, UDI/DI case 40193489042437, Lot Number: 25DBC934; Medline Kit Number/SKU 60033123: UDI/DI each 10193489042436, UDI/DI case 40193489042437, Lot Number: 25DBT579; Medline Kit Number/SKU 60033123: UDI/DI each 10193489042436, UDI/DI case 40193489042437, Lot Number: 25FBF145; Medline Kit Number/SKU 60033123: UDI/DI each 10193489042436, UDI/DI case 40193489042437, Lot Number: 25GBJ123; Medline Kit Number/SKU 60033123: UDI/DI each 10193489042436, UDI/DI case 40193489042437, Lot Number: 25HBQ032; Medline Kit Number/SKU 60033123: UDI/DI each 10193489042436, UDI/DI case 40193489042437, Lot Number: 25IBF219; Medline Kit Number/SKU 60033123: UDI/DI each 101934890424
10193489040234, 40193489040235, 10193489042436, 40193489042437, 10193489043273, 40193489043274, 10193489044539, 40193489044530, 10193489045062, 40193489045063, 10193489045383, 40193489045384, 10193489046458, 40193489046459, 10193489046809, 40193489046800, 10193489047233, 40193489047234, 10193489047639, 40193489047630, 10193489048032, 40193489048033, 10193489050929, 40193489050920, 10193489052527, 40193489052528, 10193489053258, 40193489053259, 10193489059502, 40193489059503, 10193489059687, 40193489059688, 10193489060416, 40193489060417, 10193489062823, 40193489062824, 10193489989557, 40193489989558, 10193489189582, 40193489189583
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.