Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may disconnect during use, causing potential leakage or injury. 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 a loose or full disconnection between the syringe and manifold, which could cause leakage or injury.
The syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold. This could lead to leakage of medical fluids or potential injury if the connection becomes unstable.
Healthcare professionals using Medline medical convenience kits with specific SKUs and lot numbers are most at risk. The recall affects kits sold for laparoscopic herniorrhaphy, minor procedures, and lap pack applications.
Check for Medline medical convenience kits labeled with SKUs DYNJ63021B, DYNJ64297B, or DYNJ82411. Affected kits have specific lot numbers: 26AMD887, 26AMA970, or 25IMB049.
Immediately stop using any Medline medical convenience kits with the specified SKUs and lot numbers as they may disconnect during use.
The NAMIC Angiographic Rotating Adaptor syringes may unwind during use, causing a loose or full disconnection between the syringe and manifold, which could lead to leakage or injury.
Kits with SKUs DYNJ63021B (Laparoscopic Herniorrhaphy), DYNJ64297B (Lap Pack), and DYNJ82411 (Minor Procedure Pack) and specific lot numbers: 26AMD887, 26AMA970, or 25IMB049.
The recall does not specify a return process, so contact Medline directly for instructions on how to handle affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1722-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1722-2026 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.
