Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot numbers listed in the recall notice.
Incomplete seals on sterile product
Stryker is recalling Daig Livewire Steerable catheters due to incomplete sterile seals. This could lead to contamination or infection risks during medical procedures if the device is used improperly.
Incomplete seals on the sterile catheter could allow contaminants to enter the device during use, potentially leading to infections or other complications during medical procedures. This is a risk specific to the sterile environment of medical settings.
Healthcare professionals using the Daig Livewire Steerable catheter for electrophysiology procedures are most at risk. Patients receiving these catheters during medical treatments may be affected if the device is used without proper sterility.
Check for the product number 401575 and lot numbers listed in the recall notice (e.g., 2696145, 3794476, 4262195, etc.). The catheter is used in electrophysiology procedures and is sold under the Daig brand.
Verify the product number (401575) and lot numbers (e.g., 2696145, 3794476) to confirm if your catheter is affected.
The recall is due to incomplete seals on the sterile product, which could lead to contamination during medical procedures.
Check for product number 401575 and lot numbers listed in the recall notice (e.g., 2696145, 3794476).
The recall does not specify a remedy, so contact Stryker directly for guidance on next steps.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2186-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2186-2026 from Stryker. 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.
