Merit Medical recalls Custom Inflation Kit models K05-00761F to K05T-03201 due to risk of handle detaching during medical procedures.
Inflation device handle may detach from the syringe during procedure.
Merit Medical is recalling specific Custom Inflation Kit models because the inflation device handle may detach during medical procedures. This could lead to complications if the handle becomes dislodged while in use.
The inflation device handle can detach from the syringe during medical procedures. If this happens, it could cause the device to become dislodged, potentially leading to complications during treatment.
Medical professionals using the recalled Custom Inflation Kits for procedures are most at risk. Patients using these kits during medical treatments may also be affected.
Check the product model numbers listed: K05-00761F, K05-01717B, K05-02080D, K05-02090C, K05-02221, K05-02338, K05-02470, and other variants. The product was sold with specific reference numbers and lot numbers listed in the recall notice.
Verify your Custom Inflation Kit model number against the list of recalled models: K05-00761F, K05-01717B, K05-02080D, K05-02090C, K05-02221, K05-02338, K05-02470, and other variants.
Reach out to Merit Medical Systems, Inc. for further assistance or to confirm if your specific model is affected.
The affected models include K05-00761F, K05-01717B, K05-02080D, K05-02090C, K05-02221, K05-02338, K05-02470, and other variants as listed in the recall notice.
The inflation device handle may detach from the syringe during medical procedures, which could lead to complications.
No, but you should check if your model is on the recall list and contact Merit Medical for guidance.
We’ve drafted a message you can send Merit Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1126-2026 — Merit Medical Merit Medical Hello, I own a Merit Medical that is covered by recall Z-1126-2026 from Merit 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.
