Stry: BW Lasso 2515 NAV eco Diagnostic EP Catheter Recall: Testing Failure
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.
Recall notice
Diagnostic electrophysiology (EP) catheters do not meet testing requirements.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/55134-stry-bw-lasso-2515-nav-eco-diagnostic-ep-catheter-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/55134-stry-bw-lasso-2515-nav-eco-diagnostic-ep-catheter-recall · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2268-2024
Cite this page
“Stry: BW Lasso 2515 NAV eco Diagnostic EP Catheter Recall: Testing Failure.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/55134-stry-bw-lasso-2515-nav-eco-diagnostic-ep-catheter-recall. Based on FDA recall #Z-2268-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2268-2024%22&limit=1).
Why it’s dangerous
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.
Who’s affected
Healthcare professionals using these catheters for electrophysiology procedures are most at risk. Patients receiving these catheters during procedures may be affected.
How to tell if you have this one
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.
- Brand
Stryker Sustainability Solutions- Category
Medical device
What to do — step by step
Check Product Details
Verify the catheter model, serial numbers, and UDI code to confirm if it's affected.
How this recall unfolded
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-2268-2024 (May 10, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2268-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.