Stryker recalls Endotrac EPF/EGR Triangle Blade (Catalog 305: 01398, 01465, 01481) due to potential compromised sterile bag seals. This could risk infection during surgery.
The seal integrity of the sterile bag containing the kits may be compromised.
Stryker is recalling Endotrac EPF/EGR Triangle Blades with specific lot numbers because the sterile packaging might not seal properly. This could lead to infection if the blades are used in surgery without proper sterility.
The sterile bag containing the surgical kits may not seal correctly, potentially allowing contamination. This could lead to infections during surgery if the blades are not properly sterilized.
Surgical patients and medical professionals who use the Endotrac EPF/EGR Triangle Blades with lot numbers 01398, 01465, or 01481. Patients undergoing plantar fasciitis or related procedures are most at risk.
Check the lot number on the packaging: 01398, 01465, or 01481. The product is the Endotrac EPF/EGR Triangle Blade with catalog number 3054-1.
Look for lot numbers 01398, 01465, or 01481 on the packaging.
The recall states the sterile bag seal may be compromised, which could lead to infection. Do not use the product if you have the affected lot numbers.
The recall does not specify a remedy, so contact Stryker directly for guidance.
Check the lot number on the packaging: 01398, 01465, or 01481 for the Endotrac EPF/EGR Triangle Blade (catalog number 3054-1).
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2417-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2417-2019 from Stryker. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
