Medline Industries, LP: Namic Preceptor Manifold, custom, Medline Product
Recall reason: Medline has identified the presence of particulate within the fluid path of the Manifolds.. Recalled by Medline Industries, LP. Distribution: US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.. Classification (Class I — serious health hazard). Affected lots/dates: UDI/DI each 10193489059205, UDI/DI case 30193489059209, Lot Numbers: 117277, 119982, 122210, 122199, 130129, 133014, 13. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.
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