Stryker recalls Endotrac EPF/EGR Hook/Triangle Blade Kit (Catalogue 3056-1) due to potential compromised sterile bag seals. Affected units include specific lot numbers. Consumers should contact Stryker for details.
The seal integrity of the sterile bag containing the kits may be compromised.
Stry:ker is recalling Endotrac EPF/EGR Hook/Triangle Blade Kits with catalogue number 3056-1 because the sterile bags might not seal properly. This could lead to contamination risks during medical procedures. Affected units have specific lot numbers.
The sterile bags that hold the surgical kits may not seal correctly, potentially allowing contamination. This could happen during medical procedures if the kit is used without proper sterility.
Medical professionals using the Endotrac kits for surgical procedures are most at risk. Patients receiving these kits could face contamination if the sterile bags are compromised.
Check for catalogue number 3056-1 on the kit packaging. Affected units include specific lot numbers: 01404 and 01478.
Reach out to Stryker directly for specific instructions on how to handle affected kits.
The recall is for potential contamination risk if the sterile bag seals are compromised, but no specific injuries have been reported.
Lot numbers 01404 and 01478 are affected.
The recall does not require immediate stop use; contact Stryker for specific instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1849-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1849-2019 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.
