Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may disconnect during use. Affected kits have specific SKUs and lot numbers. Stop using immediately to prevent injury.
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 NAM:Angiographic Rotating Adaptor syringes. These syringes may disconnect during use, potentially causing injury. Affected kits have specific SKUs and lot numbers listed in the recall notice.
The syringe rotating adaptor may unwind during use, leading to a loose or full disconnection between the syringe and manifold. This disconnection could cause injury if the syringe is not securely attached during medical procedures.
Healthcare workers using Medline medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes are most at risk. Patients receiving injections with these syringes could also be affected.
Check for Medline medical convenience kits labeled 'GLOVE PACK 7.0 (15PK)' with SKU # DYNJ63673D. The lot number 25GLA141 and UDI/DI numbers 10195327304843 and 40195327304844 are also associated with this recall.
Discontinue use of the recalled medical convenience kits to prevent potential disconnection and injury.
The recalled syringes are NAMIC Angiographic Rotating Adaptor (RA) Control Syringes with SKU # DYNJ63673D.
Check for the label 'GLOVE PACK 7.0 (15PK)' with SKU # DYNJ63673D and lot number 25GLA141.
The recall does not mention a fix; the remedy is null, so users must stop using the affected kits immediately.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1725-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1725-2026 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.
