Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may disconnect during use, causing potential leaks or injury. Affected kits include Shoulder Arthroscopy and Extremity Packs 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 medical convenience kits that include NAMIC Angiographic Rotating Adaptor syringes. The syringes may rotate loose during use, potentially disconnecting from the manifold and causing leaks or injury.
The syringe rotating adaptor may unwind during use, leading to a loose or full disconnection between the syringe and manifold. This can cause leaks or potential injury if the syringe is used improperly.
Healthcare professionals using Medline medical convenience kits with the specific SKUs and lot numbers listed in the recall. Those handling the syringes during medical procedures are most at risk.
Check for Medline medical convenience kits labeled as Shoulder Arthroscopy Pack (SKU # DYNJ30880M) or Extremity Pack (SKU # DYNJ64295A). The affected kits have specific lot numbers: 25LMJ532 for the Shoulder Arthroscopy Pack and 24KMI274 for the Extremity Pack.
Look for the specific SKU numbers and lot numbers listed in the recall to identify affected kits.
If you have the affected kits, stop using them immediately to prevent potential disconnection and injury.
The syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold, which could lead to leaks or injury.
Shoulder Arthroscopy Pack (SKU # DYNJ30880M) and Extremity Pack (SKU # DYNJ64295A) with lot numbers 25LMJ532 and 24KMI274 respectively.
The recall 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-1730-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1730-2026 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.
