Class IOngoingZ-2146-2026
Medline Industries, LP recalls Medline medical convenience kits
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
Class I recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 97–108 of 595 recalls
Class IOngoingZ-2145-2026
Medline Industries, LP recalls 1. 3 VALVE MAN KIT
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
Class IOngoingZ-2144-2026
Medline Industries, LP recalls 1. DBD-MTS
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
Class IOngoingZ-2143-2026
Medline Industries, LP recalls Medline medical convenience kits
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
Class IOngoingZ-2142-2026
Medline Industries, LP recalls Namic Preceptor Manifold
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
Class IOngoingZ-2141-2026
Medline Industries, LP recalls Namic Preceptor Manifold
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline Industries, LPILMay 20, 2026
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
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-2066-2026
Windstone Medical Packaging, Inc. recalls Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes…
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between…
Windstone Medical Pack…MTMay 20, 2026
Class IOngoingZ-2047-2026
Omnicell, Inc. recalls Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028
Potential for mislabeled syringe produced by the i.v.STATION device.
Omnicell, Inc.PAMay 20, 2026
Class IOngoingZ-2007-2026
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
Medical Action Industr…NCMay 13, 2026