Stryker recalls BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters (REF D134301) due to failing electrophysiology testing requirements. Affected units have specific serial numbers and UDI codes.
Diagnostic electrophysiology (EP) catheters do not meet testing requirements.
Stryker is recalling BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters because they don't meet required testing for electrophysiology procedures. This could lead to improper medical use if the catheters fail during procedures.
The catheters do not meet testing requirements for electrophysiology procedures. This could mean they might not function properly during critical medical procedures, potentially causing harm to patients.
Healthcare professionals using these catheters for electrophysiology procedures are most at risk. Patients receiving these catheters during procedures may be affected.
Check for the model 'BW Lasso 2515 NAV eco Variable Diagnostic EP Catheter' with serial numbers 4175411, 4202651, 4116975, 4202652, 4175410, or 4175402. The UDI code starts with 00885825011680.
Verify the catheter model, serial numbers, and UDI code to confirm if it's affected.
The catheters do not meet testing requirements for electrophysiology procedures.
The recall record does not specify a remedy, so contact Stryker Sustainability Solutions for guidance.
Check for the model 'BW Lasso 2515 NAV eco Variable Diagnostic EP Catheter' with serial numbers 4175411, 4202651, 4116975, 4202652, 4175410, or 4175402. The UDI code starts with 00885825011680.
We’ve drafted a message you can send Stryker Sustainability Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-2268-2024 — Stryker Sustainability Solutions Stryker Sustainability Solutions Hello, I own a Stryker Sustainability Solutions that is covered by recall Z-2268-2024 from Stryker Sustainability Solutions. 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.
