Critical Alert
Medline Industries Recalls Medline medical convenience kits
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #Z-2143-2026Medical Device
Medline Industries Recalls Medline medical convenience kits
Medline Industries, LP · Class I — Most Serious
Product Description
Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C; 2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185; 3. ANGIO KIT, Medline Kit Number/SKUVASC1057.
Reason for Recall
Medline has identified the presence of particulate within the fluid path of the Manifolds.
FDA Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
Sources: FDA openFDA Enforcement Database