Medline recalls NAMIC Angiographic Syringes (various sizes) due to potential rotation of the adaptor during use, which may cause loose connections or disconnection from the 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 NAMIC Angiographic Syringes (multiple sizes) because the syringe's rotating adaptor can unwind during use, potentially causing a loose or full disconnection between the syringe and manifold. This could lead to improper function or injury during medical procedures.
The syringe's rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold. This could lead to improper function or injury during medical procedures if the connection is not secure.
Healthcare professionals and medical facilities that own or use the recalled NAMIC Angiographic Syringes (specific models and lot numbers listed in the recall) are most at risk.
Check the product label for the model and lot numbers listed in the recall. The affected syringes include specific sizes (20ml, 10ml, 12ml) with Medline SKUs 70075027 through 80097107 and the listed lot numbers.
Look for the model and lot numbers on the syringe label to determine if it is affected.
Reach out to Medline for further assistance or to confirm if your syringe is affected.
The recall includes NAMIC Angiographic Syringes with specific sizes (20ml, 10ml, 12ml) and Medline SKUs 70075027 through 80097107.
Check the product label for the model and lot numbers listed in the recall. Affected syringes have specific Medline SKUs and lot numbers.
Contact Medline directly for further assistance or to confirm if your syringe is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1712-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1712-2026 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.
