Class IOngoingZ-2140-2026
Medline Industries, LP recalls Namic Angiographic Manifold
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–6 of 6 recalls
Class IOngoingZ-2139-2026
Medline Industries, LP recalls Namic Angiographic Manifold
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
Class IOngoingZ-2138-2026
Medline Industries, LP recalls Namic Angiographic Manifold
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
Class IOngoingZ-1715-2026
Medline Industries, LP recalls Medline medical convenience kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the s…
Medline Industries, LPILApr 15, 2026
Class IIOngoingZ-0533-2026
Merit Medical Systems, Inc. recalls PhD Hemostasis Valve
Hemostasis valve has a manufacturing defect and when used the valve cap may remain depressed, leading to potential leakage, which may result in procedure inconvenience and/or hemorrhage.
Merit Medical Systems,…UTNov 26, 2025
Class IIOngoingZ-2553-2025
Merit Medical Systems, Inc. recalls 10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / 00884450821305 MAPTE…
Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the fluid pathway.
Merit Medical Systems,…UTSep 17, 2025