AVID Medical recalls Halyard CARDIAC CATH TRAY SHANDS JAX kits (models SHND401-04 and SHND401-05) due to potential risk of medline syringe rotating adaptor unwinding, which may cause loose or full disconnection between syringe and manifold.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
AVID Medical is recalling two specific models of Halyard CARDIAC CATH TRAY SHANDS JAX kits because the syringe rotating adaptor may unwind during use, leading to a loose or full disconnection between the syringe and manifold. This could cause medical complications during procedures.
The medline syringe rotating adaptor in these kits may unwind during use, causing a loose or full disconnection between the syringe and manifold. This could lead to medical complications during procedures if the connection is not properly maintained.
Healthcare professionals using the Halyard CARDIAC CATH TRAY SHANDS JAX kits with model numbers SHND401-04 or SHND401-05 are most at risk. Patients receiving procedures using these kits could be affected if the connection becomes loose or disconnected.
Check for model numbers SHND401-04 or SHND401-05 on the kit. The UDI-DI (kit lot numbers) for SHND401-04 include specific numbers like 1577749, 1577750, and others listed in the recall notice. For SHND401-05, the UDI-DI lot numbers include 1652367, 1668844, and others.
Identify the model number on the kit, which should be SHND401-04 or SHND401-05.
Check the UDI-DI (kit lot numbers) listed in the recall notice for your specific model.
The medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold, which could lead to medical complications.
Model numbers SHND401-04 and SHND401-05 are affected, with specific UDI-DI lot numbers listed in the recall notice.
The recall does not require immediate stop use; healthcare professionals should check the model and lot numbers and take appropriate action if affected.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1972-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1972-2026 from AVID Medical. 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.
