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 that contain NAMIC Angiographic Rotating Adaptor syringes. These syringes may unwind during use, leading to loose or full disconnections between the syringe and manifold, which could cause medical errors.
The syringe 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 connection fails during procedures.
Healthcare professionals using these kits for medical procedures are most at risk. The recall affects Medline medical convenience kits with specific SKUs and lot numbers.
Check for Medline medical convenience kits labeled with specific SKUs: VASC1061, VASC1074, VASC1198, VASCSHPOFF1, or VASCSLPON1. Also look for lot numbers like 25IBN161, 25GBF769, 25HBN798, etc.
Look for the specific Medline SKU and lot number on the kit label to confirm if it's affected.
If you have the affected kits, stop using them immediately to prevent potential disconnections during medical procedures.
The syringe rotating adaptor may unwind during use, causing a loose connection or full disconnection between the syringe and manifold, which could lead to medical errors.
Affected kits include those with SKUs VASC1061, VASC1074, VASC1198, VASCSHPOFF1, or VASCSLPON1 and specific lot numbers like 25IBN161, 25GBF769, 25HBN798, etc.
The recall record does not specify a return process, so contact Medline directly for instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1715-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1715-2026 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.
