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Medline Industries, LP: Namic Preceptor Manifold, custom, Medline Product

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

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 10193489059137, UDI/DI case 30193489059131, Lot Numbers: 89181, 95326, 95254, 102287, 102286, 102706, 10536. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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