Stryker recalls specific end cap implants due to potential blister pack contamination. This could compromise sterility during surgery. Affected units have catalog number 18300015S and lot number K037E2D.
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Stryker is recalling certain end cap implants for potential contamination. If the blister pack isn't sealed properly, the implants could become contaminated during surgery, risking infection or other complications.
The blister pack that holds the implant may become compromised, meaning the sterile environment is no longer maintained. This could lead to contamination of the implant during surgical procedures, potentially causing infection or other complications.
Stryker End Cap T2 Humerus implants with catalog number 18300015S and lot number K037E2D are affected. Surgeons and medical facilities using these implants for bone fixation are most at risk.
Check for the catalog number 18300015S and lot number K037E2D on the implant packaging. These implants are single-use devices for temporary bone fixation.
Look for the catalog number 18300015S and lot number K037E2D on the implant packaging.
The recall is due to potential compromise of the blister pack's seal, which could lead to contamination of the implant and compromise sterility during surgery.
Check the packaging for the catalog number 18300015S and lot number K037E2D. If you have these identifiers, contact Stryker for further instructions.
The recall indicates a potential risk of contamination, so it is not safe to use without verifying the packaging details and following the manufacturer's instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2378-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2378-2020 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.
