Medline recalls medical convenience kits with Namic Manifold due to particulate in fluid path. Affected kits have specific lot numbers and model codes. Stop using immediately to prevent potential blockages.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline is recalling medical convenience kits that contain Namic Manifolds because they may have particulate in the fluid path. This could cause blockages during medical procedures, so affected users should stop using the kits immediately.
Particulate in the fluid path of the Namic Manifold could block medical equipment during procedures. This might lead to complications like failed treatments or injuries if the blockage occurs in critical areas.
Healthcare professionals using Medline medical convenience kits for angiography or catheter labs are most at risk. Patients receiving procedures with these kits could face complications if particulate causes blockages.
Check for Medline kits labeled 'ANGIOGRAPHY CATH LAB' or 'CATH LAB PACK' with specific lot numbers: 25DMA809, 23GBA252, 23HBI873, 23IBR043, 23KBF277, or 24ABQ959. The kit numbers include SKUDYNJ23532C, SKUDYNJ65185, and SKUVASC1057.
Discontinue use of all affected Medline medical convenience kits to prevent potential blockages during procedures.
The hazard is particulate in the fluid path of the Namic Manifold, which could cause blockages during medical procedures.
Kits labeled 'ANGIOGRAPHY CATH LAB' (SKUDYNJ23532C), 'CATH LAB PACK' (SKUDYNJ65185), and 'ANGIO KIT' (SKUVASC1057) with specific lot numbers.
Check the lot number on the kit: 25DMA809, 23GBA252, 23HBI873, 23IBR043, 23KBF277, or 24ABQ959 for the affected models.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2143-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2143-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
