Stryker recalls Endotrac EPF/EGR Triangle Blade (Catalog 305:4A-1) due to potential compromised sterile bag seals. This could lead to infection risks during surgery. Affected units sold with lot number 01411.
The seal integrity of the sterile bag containing the kits may be compromised.
Stryker is recalling Endotrac EPF/EGR Triangle Blades (Catalog Number 3054A-1) because the sterile packaging might not seal properly. This could increase infection risk during surgery if the blades are used without proper sterility.
The sterile bag containing the surgical kits might not seal correctly, potentially allowing contamination. This could lead to infections during surgery if the blades are not properly sterilized.
Medical professionals who use the Endotrac EPF/EGR Triangle Blades for plantar fasciitis surgery are most at risk. Patients receiving this surgical treatment may be affected if the blades are used without proper sterility.
Check for the catalog number 3054A-1 on the blade packaging. The recall affects units sold with lot number 01411. The blades are used for plantar fasciitis surgery.
Look for the catalog number 3054A-1 and lot number 01411 on the blade packaging.
The sterile bag containing the surgical kits may have compromised seal integrity, potentially leading to contamination during surgery.
Check the packaging for catalog number 3054A-1 and lot number 01411. If you have the affected units, contact Stryker for further instructions.
The recall is due to potential contamination risks during surgery, not direct injury risks. The hazard level is low risk.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2422-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2422-2019 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.
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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.
