Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may disconnect during use, causing potential leaks or injury. Affected kits have 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 include NAMIC Angiographic Rotating Adaptor syringes. The syringes may unwind during use, leading to a loose or full disconnection between the syringe and manifold, which could cause leaks or injury.
The syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold. This could lead to leaks or potential injury if the connection is not secure.
Healthcare professionals and medical facilities using the recalled Medline convenience kits are most at risk. The specific kits contain NAMIC syringes with certain SKUs and lot numbers.
Check for Medline convenience kits labeled with SKU # DYNJ42892F or DYNJ42892G. The affected kits have specific lot numbers listed in the recall notice.
Immediately stop using any Medline convenience kits with the listed SKUs and lot numbers to prevent potential disconnection and injury.
The NAMIC Angiographic Rotating Adaptor syringes may unwind during use, causing a loose or full disconnection between the syringe and manifold, which could lead to leaks or injury.
Kits with SKU # DYNJ42892F or DYNJ42892G, including specific lot numbers listed in the recall notice.
The recall does not specify a return process; you should stop using the affected kits immediately.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1727-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1727-2026 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.
