Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may unwind, causing loose connections or full disconnection. 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 containing NAMIC Angiographic Rotating Adaptor syringes because the rotating adaptor may unwind during use, leading to loose or full disconnection between the syringe and manifold. This could cause medical errors if the syringe becomes disconnected during procedures.
The rotating adaptor may unwind during use, creating a loose connection or full disconnection between the syringe and manifold. This could lead to medical errors if the syringe becomes disconnected during procedures.
Healthcare professionals using these medical kits are most at risk, particularly during procedures requiring precise syringe connections.
Check for Medline medical convenience kits with specific SKUs: DYNJ68037C, DYNJ89845, or DYNJ89845A. Lot numbers include 25HBV397, 25CBU222, 25BBC195, 25ABI611, 25LBK402, 25KBH371, and 25IBK975.
Identify the SKU and lot number on the kit to confirm if it's affected.
Reach out to Medline for guidance on next steps if the kit is affected.
The rotating adaptor may unwind during use, causing a loose connection or full disconnection between the syringe and manifold.
Kits with SKUs DYNJ68037C, DYNJ89845, or DYNJ89845A and specific lot numbers including 25HBV397, 25CBU222, 25BBC195, 25ABI611, 25LBK402, 25KBH371, and 25IBK975.
The recall does not require immediate stop use; healthcare professionals should check kit details and contact Medline for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1719-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1719-2026 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.
