Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may disconnect during use, causing potential leakage or injury. Affected kits include specific SKUs and lot numbers.
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 syringe and manifold.
Medline is recalling medical convenience kits that contain NAMIC Angiographic Rotating Adaptor syringes. The recall is due to a risk that the syringe adapter may unwind during use, leading to a loose or full disconnection between the syringe and manifold.
The syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold. This could lead to leakage of medical fluids or improper treatment delivery.
Healthcare professionals and medical facilities using the recalled kits are most at risk. Patients receiving treatments with these kits could face potential leakage or injury if the connection disconnects.
Check for the specific Medline SKUs listed in the recall: CDS780138K, DYNJ36478B, DYNJ910458, VASC1081C, and VASC1510. The kits were sold with lot numbers starting with 24 or 25.
Immediately stop using any medical convenience kits with the listed SKUs and lot numbers to prevent potential disconnection.
The syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold, which could lead to leakage or improper treatment delivery.
The affected SKUs are CDS780138K, DYNJ36478B, DYNJ910458, VASC1081C, and VASC1510.
Check the product label for the specific Medline SKUs listed in the recall and the lot numbers starting with 24 or 25.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1721-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1721-2026 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.
