AVID Medical recalls Halyard HEART CATH SELF REGIONAL kit (model SELF131-05) due to potential syringe disconnection during use. Affected units have specific lot numbers.
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 HEART CATH SELF REGIONAL kits with model number SELF131-05 because the syringe rotating adaptor may unwind, causing a loose or full disconnection between the syringe and manifold. This could lead to improper medical connections during procedures.
The syringe rotating adaptor in the kit may unwind during use, creating a loose or full disconnection between the syringe and manifold. This could result in improper medical connections during procedures, potentially affecting patient safety.
Healthcare professionals using the Halyard HEART CATH SELF REGIONAL kit for medical procedures are most at risk. Patients receiving care with this specific kit may also be affected.
Check for the model number SELF131-05 on the kit. Affected units have specific lot numbers listed in the recall notice.
Review the lot numbers provided in the recall notice to confirm if your kit is affected.
The recall addresses a potential risk of syringe disconnection during use, but the hazard is not described as causing serious injury in normal use.
Check for the model number SELF131-05 and the specific lot numbers listed in the recall notice.
The recall does not specify a remedy, so no action is required beyond checking the lot numbers.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1975-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1975-2026 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.
