Medline recalls medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes due to potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection or full disconnection between the syringe and manifold.
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 include NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. The recall is due to a potential risk that the syringe rotating adaptor could unwind during use, causing a loose or full disconnection between the syringe and manifold. This could lead to improper medical procedures if not addressed.
The syringe rotating adaptor may unwind during use, which can cause a loose or full disconnection between the syringe and manifold. This could lead to improper medical procedures if the connection is not secure, potentially affecting patient safety during procedures.
Healthcare professionals and medical facilities that use these kits are most at risk. The specific kits and their model numbers are listed in the recall notice.
Check for the following Medline medical convenience kits: MTS RH LFT HRT KIT (SKU #60010508), MTS 3V W/GUIDE (SKU #60100701), ANGIOGRAPHY KIT (SKU #60131209), and other kits listed with their specific SKUs. The recall includes specific lot numbers and UDI/DI codes.
Identify if your medical convenience kit contains any of the listed Medline SKUs and lot numbers.
Reach out to Medline for guidance on how to safely handle the recalled kits.
The recall affects Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes, including specific SKUs like MTS RH LFT HRT KIT (SKU #60010508) and others listed in the notice.
Check the Medline SKU and lot number on your kit. The recall includes specific SKUs and lot numbers listed in the notice.
Contact Medline directly for guidance on how to safely handle the recalled kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1724-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1724-2026 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.
