Reported Feb 5, 2025 · Ongoing

AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN: M00553670

Boston Scientific Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Boston Scientific Corporation · 100 Boston Scientific Way · Marlborough, MA · 01752-1234

Is this the product you have?

  • AXIOS Stent and Electrocautery-
  • Enhanced Delivery System 15mmx15mm UPNM00553670
Lot codes and dates
  • GTIN08714729979333
  • Lot Numbers
    • 32901294
    • 33223930
    • 33328461
    • 33413626
    • 33459702
    • 33686175
    • 33686176
    • 33766912
    • 33814306
    • 33825089
    • 33860266
    • 33920983
    • 33920984
    • 33930917
    • 34020982
    • 34020983
    • 34111459
    • 34111480
    • 34111481
    • 34135618
    • 34135619
    • 34136372
    • 34271635
    • 34297652
    • 34316296
Amount recalled
309 units

This recall covers 14 products

The agency filed one notice per product. You are reading one of them; the other 13 are below.

1 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.