Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may disconnect during use, causing potential leakage or injury. Affected kits have specific lot numbers and SKUs.
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 recall is due to a risk of the syringe rotating adaptor unwinding during use, which could cause a loose or full disconnection between the syringe and manifold.
The syringe rotating adaptor may unwind during use, leading to a loose or full disconnection between the syringe and manifold. This could cause leakage or potential injury if the syringe becomes disconnected during medical procedures.
Healthcare professionals using Medline medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes are most at risk. The recall affects kits sold with specific lot numbers and SKUs.
Check for Medline medical convenience kits labeled with SKU # DYNJ84472. Affected kits have lot numbers 23LBN016, 23KBL255, 23HBL885, or 23FBV799.
Look for SKU # DYNJ84472 on the kit label to identify affected products.
If you have the affected kits, stop using them immediately to prevent potential disconnection.
The syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold, which could lead to leakage or injury.
Affected kits have lot numbers 23LBN016, 23KBL255, 23HBL885, or 23FBV799.
Check for Medline medical convenience kits labeled with SKU # DYNJ84472 and lot numbers 23LBN016, 23KBL255, 23HBL885, or 23FBV799.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1729-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1729-2026 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.
