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 SKU 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 syringes may rotate loose during use, potentially disconnecting from the manifold and causing leaks or injury.
The syringe rotating adaptor may unwind during use, leading to a loose or full disconnection between the syringe and manifold. This could cause leaks of medical fluids or improper administration of treatments.
Healthcare workers using Medline medical convenience kits with the specific SKU numbers listed in the recall. Patients receiving care with these kits may be at risk if the syringes disconnect.
Check for Medline medical convenience kits labeled with SKU # DYNJ86596. Look for lot numbers 24FMI029 or 24DMK138 on the packaging or documentation.
Look for SKU # DYNJ86596 and lot numbers 24FMI029 or 24DMK138 on the kit packaging.
The syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold, which could lead to leaks or improper treatment.
Check for Medline medical convenience kits labeled with SKU # DYNJ86596 and lot numbers 24FMI029 or 24DMK138.
The recall does not specify a remedy, so contact Medline directly for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1723-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1723-2026 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.
