Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may unwind, causing loose or full disconnection between 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 containing NAMIC Angiographic Rotating Adaptor syringes due to a risk of the syringe rotating adaptor unwinding during use. This could lead to a loose or full disconnection between the syringe and manifold, potentially causing medical complications.
The syringe rotating adaptor may unwind during use, creating a loose or full disconnection between the syringe and manifold. This could lead to medical complications if the connection is not secure during procedures.
Healthcare professionals using Medline medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes are most at risk. The recall affects specific lot numbers and SKUs of these kits.
Check for Medline medical convenience kits labeled as 'ROBOTIC PACK' (SKU DYNJ58475F) or 'URO/GEN ROBOTIC PACK' (SKU DYNJ60803J). Look for specific lot numbers listed in the recall notice.
Look for the product label with SKU numbers DYNJ58475F or DYNJ60803J and associated lot numbers.
The syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold, which could lead to medical complications.
Check for Medline medical convenience kits labeled as 'ROBOTIC PACK' (SKU DYNJ58475F) or 'URO/GEN ROBOTIC PACK' (SKU DYNJ60803J) with specific lot numbers listed in the recall notice.
Check the kit label for SKU numbers and lot numbers. If you have a recalled kit, contact Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1728-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1728-2026 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.
