Boston Scientific recalls specific lots of Guider Softip Guide Catheters 8F 90CM due to incorrect tip curve shape. Affected products may have different tip curve than labeled. Check lot numbers for recall.
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.
Boston Scientific is recalling certain lots of Guider Softip Guide Catheters 8F 90CM because they have an incorrect tip curve shape compared to what's labeled. This could affect medical procedures where precise tip shape is critical.
The catheters have a tip curve shape that differs from what's labeled. This could cause improper positioning during medical procedures, potentially leading to complications if the catheter doesn't move as intended.
Cardiac catheter patients and medical professionals using these specific lots of Guider Softip Guide Catheters 8F 90CM. The risk is low as the issue is about tip curve shape, not immediate safety hazards.
Check the product's lot numbers: 25651745, 25651749, 25651755, 25761258, 25914835, and other specific numbers listed in the recall notice. The product is a cardiac guide catheter with catalog number H965100480.
Look for the lot numbers listed in the recall notice: 25651745, 25651749, 25651755, 25761258, 25914835, and other specific numbers.
Stryker Neurovascular observed that certain lots of Guider Softip XF Guide Catheters have an incorrect tip curve shape compared to what's labeled.
Check the lot numbers against the list provided in the recall notice to see if your product is affected.
The recall notice does not specify a remedy, only that affected products have an incorrect tip curve shape.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0014-2024 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0014-2024 from Boston Scientific. 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.
