Stryker recalls Endotrac ECTR Hook Blade (Catalog 2:055-1) due to potential compromised sterile bag seals. This could risk infection during surgery. Affected units include specific lot numbers.
The seal integrity of the sterile bag containing the kits may be compromised.
Stryker is recalling Endotrac ECTR Hook Blade surgical kits because the sterile packaging might not stay sealed properly. This could lead to infections if the kit is used without being properly sterilized.
The sterile bag that holds the surgical kits might not stay sealed correctly. If the seal is broken, the kit could become contaminated and cause infection during surgery.
Surgical professionals using the Endotrac ECTR Hook Blade for plantar fasciosis treatment. Those with specific lot numbers 01409 or 01476 are most at risk.
Check the catalog number on the product, which is 2055-1. Look for lot numbers 01409 or 01476 on the packaging.
Verify the catalog number is 2055-1 and lot numbers are 01409 or 01476.
The sterile bag seal may be compromised, potentially leading to infection if the kit is not properly sterilized.
Check for catalog number 2055-1 and lot numbers 01409 or 01476 on the packaging.
The recall record does not specify a remedy, so contact Stryker directly for guidance.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2415-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2415-2019 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.
