Reported Oct 11, 2023 · Ongoing

Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter

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 · 1 Scimed Pl · Maple Grove, MN · 55311-1565

Is this the product you have?

  • Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter
Lot codes and dates
  • GTIN 08714729202462
  • Lot/Batch Numbers

    73 of 73 codes

    • 25651700
    • 25651701
    • 25651702
    • 25651703
    • 25651704
    • 25651705
    • 25651706
    • 25651708
    • 25651709
    • 25651710
    • 25651711
    • 25761340
    • 25761341
    • 25761342
    • 25761343
    • 25964544
    • 25964545
    • 25964546
    • 25964547
    • 26019585
    • 26019586
    • 26034354
    • 26034357
    • 26138841
    • 26138842
    • 26138844
    • 26338705
    • 26338706
    • 26338707
    • 26338708
    • 26411750
    • 26411751
    • 26411752
    • 26745645
    • 26745646
    • 26891497
    • 27269743
    • 27654465
    • 27696356
    • 27703700
    • 27809357
    • 27996305
    • 26019584
    • 28107548
    • 28158175
    • 26019587
    • 28502663
    • 28502664
    • 28502665
    • 28584619
    • 28737891
    • 28737892
    • 28737893
    • 28795036
    • 28886611
    • 28886612
    • 29112775
    • 29112777
    • 26138843
    • 26138845
Amount recalled
4990 units

This recall covers 16 products

The agency filed one notice per product. You are reading one of them; the other 15 are below.

3 more are in the archive.

Where it was sold

  • Nationwide
  • IN

Why it was recalled

Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape.

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, 6:21 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.