Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to infection during medical procedures. Affected units have specific product numbers and lot codes.
Incomplete seals on sterile product
Stryker is recalling Daig Livewire Steerable catheters due to incomplete sterile seals. This could cause infections during medical procedures if the catheter is used improperly.
Incomplete seals on the catheter could allow contaminants to enter the sterile field during medical procedures. This increases the risk of infection for patients undergoing electrophysiology treatments.
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 product number 401652 and lot numbers listed in the recall notice. The catheter is used in medical procedures for electrophysiology treatments.
Verify the product number (401652) and lot numbers (3430230, 4648604, etc.) on the catheter packaging.
The catheter has incomplete seals on the sterile product, which could lead to contamination during medical procedures.
Check the product number and lot numbers listed in the recall notice to see if your catheter is affected.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2190-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2190-2026 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.
