Stryker recalls Endotrac ECTR Triangle Blade (Catalog 2054A-1) due to potential compromised sterile bag seals. This could lead to infection risks during surgery. Affected units include Lot 01408.
The seal integrity of the sterile bag containing the kits may be compromised.
Stry:ker is recalling Endotrac ECTR Triangle Blades (Catalog 2054A-1) because the sterile packaging might not seal properly. This could let bacteria enter during surgery, increasing infection risk. The recall affects specific surgical kits used for plantar fasciitis treatment.
The sterile bag that holds the surgical kits may not seal properly, allowing bacteria to enter the kit. This could lead to infections during surgery if the kit is used without proper sterility.
Surgical teams using the Endotrac ECTR Triangle Blade (Catalog 2054A-1) for plantar fasciitis procedures are affected. Patients undergoing surgery with this specific kit are at risk of infection if the sterile bag seal is compromised.
Check for the catalog number 2054A-1 on the Endotrac ECTR Triangle Blade. The affected lot number is 01408. This product is used for plantar fasciitis surgery.
Look for the catalog number 2054A-1 and lot number 01408 on the Endotrac ECTR Triangle Blade.
The recall indicates a potential risk of compromised sterile bag seals, which could lead to infection during surgery. The product is not safe to use without checking the recall details.
The recall does not specify a remedy, so check with Stryker directly for guidance on next steps.
The sterile bag may not seal properly, increasing infection risk during surgery if the kit is used without proper sterility.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2420-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2420-2019 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.
