Stryker recalls Endotrac ECTR Push Blade (Catalog 2:053-1) due to potential compromised sterile bag seals. This could lead to infection risks during plantar fasciosis treatment. Affected units include Lot 01400.
The seal integrity of the sterile bag containing the kits may be compromised.
Stryker is recalling Endotrac ECTR Push Blade kits (Catalog Number 2053-1) because the sterile packaging might not stay sealed properly. This could let bacteria get into the blades during surgery, increasing infection risk for patients getting plantar fasciosis treatment.
The sterile bag that holds the surgical kits might not stay sealed well. If the seal breaks, bacteria could enter the blades during surgery, potentially causing infections in patients.
Patients receiving plantar fasciosis treatment with the Endotrac ECTR Push Blade system are most at risk. Healthcare providers using the system may also be affected if they have the recalled lot.
Check for the catalog number 2053-1 on the product label. The affected lot number is 01400. This product is used for plantar fasciosis treatment.
Look for the catalog number 2053-1 and lot number 01400 on the product.
The recall states the sterile bag seal may be compromised, which could lead to infection risks. However, the remedy is not specified, so users should check the label for the affected lot number.
The recall record does not specify a remedy, so users should check the product label for the catalog number 2053-1 and lot number 01400. If they have the affected lot, they should contact Stryker for further instructions.
Patients receiving plantar fasciosis treatment with the Endotrac ECTR Push Blade system may face infection risks if the sterile bag seal is compromised.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2413-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2413-2019 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.
