Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor (RA) Control Syringes due to risk of unwinding, which could cause 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 that contain NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. The recall is because the syringe rotating adaptor may unwind during use, potentially causing a loose or full disconnection between the syringe and manifold.
The syringe rotating adaptor may unwind during use, which can lead to a loose or full disconnection between the syringe and manifold. This could cause medical errors during procedures if the connection is not secure.
Healthcare professionals using these medical convenience kits for catheter procedures are most at risk. The specific kits and models are listed in the recall notice with their SKUs and lot numbers.
Check the product labels for the specific Medline SKUs listed: CATH LAB PACK-LF (SKU 00-HCT055P), INTERVENTIONAL CATH LAB PK-LF (SKU DYNJ0376230Q), and other kits with the listed SKUs and lot numbers.
Look for the specific Medline SKUs and lot numbers listed in the recall notice to identify affected kits.
The syringe rotating adaptor may unwind during use, which could cause a loose or full disconnection between the syringe and manifold, potentially leading to medical errors during procedures.
Check the product labels for the specific Medline SKUs and lot numbers listed in the recall notice, such as SKU 00-HCT055P with lot numbers 24BBI341, 23LBP066, etc.
The recall notice does not specify a remedy, so contact Medline directly for guidance on how to handle the affected products.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1716-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1716-2026 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.
