Medline recalls NAMIC Angiographic Syringes with potential risk of rotating adaptor unwinding during use, causing loose connection or disconnection between syringe and manifold. Affected models include 10ml, 12ml, 20ml syringes with 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 NAMIC Angiographic Syringes that may rotate during use, potentially causing a loose or full disconnection between the syringe and manifold. This could lead to improper medical procedures if the connection fails during use.
The rotating adaptor in the syringe may unwind during use, creating a loose or full disconnection between the syringe and manifold. This could lead to improper fluid delivery or contamination if the connection fails during medical procedures.
Healthcare professionals and medical facilities using these syringes are most at risk, particularly during procedures requiring precise fluid delivery where a disconnection could cause errors.
Check for syringes labeled with specific model descriptions like 'SYRINGE,20ML,CONTROL,-,PKG' or similar, with Medline SKUs listed in the recall (e.g., 70075027, 80075027). Affected units have specific lot numbers and UDI/DI codes.
Look for the product label on the syringe that matches the descriptions in the recall, such as 'SYRINGE,20ML,CONTROL,-,PKG' or similar.
If you have the affected syringes, contact Medline directly for instructions on how to return or replace them.
Affected models include NAMIC Angiographic Syringes with specific sizes (10ml, 12ml, 20ml) and Medline SKUs listed in the recall, such as 70075027, 80075027, and others.
Check the syringe label for the product descriptions like 'SYRINGE,20ML,CONTROL,-,PKG' or similar, and verify the Medline SKU and lot number against the list provided in the recall.
No, but you should check if your syringes are affected and contact Medline for instructions on returning or replacing them.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1718-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1718-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
