AVID Medical recalls Halyard NEURO IR Peripheral (PS 64405) kits with model UINR44-01 due to potential risk of syringe rotating adaptor unwinding, causing loose connections or disconnections during use.
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 Halyard NEURO IR Peripheral (PS 64405) kits with model number UINR44-01. The risk is that 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 if the kit is used for injections.
The syringe rotating adaptor in the kit may unwind during use, which can cause a loose or full disconnection between the syringe and manifold. This disconnection could lead to medical complications such as incorrect dosing or injection failure if the kit is used for injections.
Healthcare professionals using the Halyard NEURO IR Peripheral (PS 64405) kit with model UINR44-01 for injections are most at risk. Patients receiving injections with this kit could experience complications if the connection becomes loose or disconnected.
Check for the model number UINR44-01 on the Halyard NEURO IR Peripheral (PS 64405) kit. The kit was sold with specific UDI (Kit Lot Numbers) as listed in the recall notice.
Verify the model number on the kit is UINR44-01.
Reach out to AVID Medical for further instructions on handling the recalled kit.
Yes, healthcare professionals using the Halyard NEURO IR Peripheral (PS 64405) kit with model UINR44-01 for injections are at risk of complications if the syringe rotating adaptor unwinds.
Look for the model number UINR44-01 on the Halyard NEURO IR Peripheral (PS 64405) kit. The specific UDI (Kit Lot Numbers) are listed in the recall notice.
Contact AVID Medical for instructions on handling the recalled kit. The recall does not specify a return or replacement process.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1976-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1976-2026 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.
