FDA DeviceClass INotable

FDA Recall: Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass ada

Date: 2026-05-20
Brand: Medline Industries, LP
Category: Medical Device
FDA Class: Class I

Description

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Hazard

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Remedy

7075 units

View original recall →
Share:

Related Recalls

2026-05-20 · FDA_DEVICE
FDA Recall: Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure
Medline Industries, LP
2026-05-20 · FDA_DEVICE
FDA Recall: Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medlin
Medline Industries, LP
2026-05-20 · FDA_DEVICE
FDA Recall: Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038301; Cardiopulmonary bypass ada
Medline Industries, LP
2026-05-20 · FDA_DEVICE
FDA Recall: Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure
Medline Industries, LP