Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to infection during medical procedures. Affected units include specific lot numbers and product codes.
Incomplete seals on sterile product
Stry:ker is recalling Daig Livewire Steerable catheters due to incomplete sterile seals. This could lead to infections during medical procedures if the catheters are used improperly.
Incomplete seals on the catheter could allow contamination during medical procedures. This might lead to infections if the catheter is not properly sterilized before use.
Medical professionals using the Daig Livewire Steerable catheter for electrophysiology procedures are most at risk. Patients receiving these catheters during procedures may also be affected.
Check for the product number 401923 and lot numbers 3557411, 3702628, or 4498116 on the catheter packaging or label.
Identify the product number and lot numbers 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.
The official recall notice does not specify a remedy or action for affected units.
Check for product number 401923 and lot numbers 3557411, 3702628, or 4498116 on the catheter packaging or label.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2196-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2196-2026 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.
