Stryker recalls Endotrac EPF/EGR Hook Blade (Catalog 305:1) due to potential compromised sterile bag seals. This may risk infection during surgery. Affected lot numbers: 01403, 01466, 01483.
The seal integrity of the sterile bag containing the kits may be compromised.
Stryker is recalling Endotrac EPF/EGR Hook Blades with catalog number 3055-1 because the sterile packaging might not seal properly. This could lead to infection during surgery if the blades are used without proper sterility.
The sterile bag that holds the blades might not seal correctly, which could allow contamination. If the bag isn't sterile, using the blades during surgery might cause infection.
Surgical patients and medical professionals using the Endotrac EPF/EGR Hook Blades for plantar fasciosis or gastrocnemius equinus treatment. Patients undergoing surgery with these blades are most at risk.
Check the catalog number on the blade packaging. Affected items have catalog number 3055-1 and lot numbers 01403, 01466, or 01483.
Look for catalog number 3055-1 on the blade packaging.
This recall affects surgical patients and medical professionals using the Endotrac EPF/EGR Hook Blades for plantar fasciosis or gastrocnemius equinus treatment.
Lot numbers 01403, 01466, and 01483.
Check the catalog number on the packaging; affected items have catalog number 3055-1 and the listed lot numbers.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2418-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2418-2019 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.
